Hospira Inc. recalls

102 recalls on record · latest: May 22, 2024

Official U.S. recall history for Hospira Inc., compiled from official government records.

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Hospira Inc. recalls Hospira — Buprenorphine Hydrochloride Injection Carpuject Units and Labetalol Hydrochloride Injection, USP Carpuject U…

May 22, 2024 · Pet food & animal recalls Device & Drug Safety – Potential Packaging Defect — Defect

Hospira product recalled over foreign material

October 2, 2023 · Drug & medication recalls Potential Presence of Glass Particulates — Potential Foreign Material

Hospira product recalled over labeling errors

May 4, 2021 · Drug & medication recalls Due to mislabeling — Device & Drug Safety

Sterile Water for Injection recalled over foreign material

May 4, 2021 · Drug & medication recalls Due to visible particulate — Potential Foreign Material

Hospira, Inc. recalls Hospira, Inc. — Hydromorphone HCL Injection, USP

April 13, 2020 · Drug & medication recalls Due to The Potential for Empty or Cracked Glass Vials — Damage

Hospira Inc. recalls Hospira Inc. — Bacteriostatic Water for Injection

September 6, 2019 · Pet food & animal recalls Potential Lack of Sterility Assurance — Potential Lack of Sterility

Sodium bicarbonate injection USP recalled over foreign material

March 15, 2019 · Drug & medication recalls Presence of Particulate Matter — Potential Foreign Material

Hospira Inc. recalls Hospira — Daptomycin for Injection 500 mg, Lyophilized Powder For Solution, Single Dose Vial

June 27, 2018 · Drug & medication recalls Adverse event reports indicative of infusion reactions — Defect

Naloxone Hydrochloride Injection recalled over foreign material

June 4, 2018 · Drug & medication recalls Potential of Foreign Material — Potential Foreign Material

Hospira, Inc. recalls Hospira, Novaplus — Labetalol Hydrochloride Injection, USP

February 23, 2018 · Drug & medication recalls Due to Potential Of Cracked Glass At The Rim Surface Of The Vials — Damage

25% Dextrose Injection recalled over foreign material

February 8, 2018 · Drug & medication recalls Due to the Presence of Particulate Matter — Potential Foreign Material

Hospira, Inc. recalls HYDROmorphone, Levophed — Hydromorphone HCl, Levophed

February 6, 2018 · Drug & medication recalls Due to Lack of Sterility Assurance — Potential Lack of Sterility

Hospira, Inc. recalls Hospira, Inc. — Vancomycin Hydrochloride for Injection

August 30, 2017 · Drug & medication recalls Due to the Presence of Particulate Matter — Device & Drug Safety

Hospira Inc. recalls Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospi…

April 21, 2017 · Drug & medication recalls High risk Presence of Particulate Matter: human hair found within an internal sample syri…

Fentanyl Citrate Injection recalled over sterility concerns

November 1, 2016 · Drug & medication recalls Moderate risk Lack of Assurance of Sterility: Complaints of broken tips on the ampules.

Hospira Inc. recalls DOBUTamine Injection, USP 250 mg/20 mL, 20 mL Vial, For IV Use Only, Must be Diluted Prior to Use, (12.5 mg per mL), Rx…

August 15, 2016 · Drug & medication recalls Moderate risk Discoloration: Firm received complaints of product discoloration and particulat…

Hospira Inc. recalls 5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia…

June 29, 2016 · Drug & medication recalls Failed Stability Specifications: The recalled lots did not meet the specificati…

Hospira Inc. recalls Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32

June 23, 2016 · Drug & medication recalls Moderate risk Crystallization: Product contains particulate identified to be crystallized act…

Hospira Inc. recalls Vancomycin Hydrochloride for Injection, USP, 10 g, 100 mL vial, Rx only, Hospira, Lake Forest, IL, NDC 0409-6510-01

May 6, 2016 · Drug & medication recalls Moderate risk Presence of Particulate Matter: Cardboard

Hospira Inc. recalls The Plum A+ is a dual-line volumetric infusion system designed to meet the growing demand for hospital-wide, as well as…

March 25, 2016 · Medical device recalls Moderate risk Firm's investigation determined that the Proximal Occlusion Alarms observed in…

Hospira Inc. recalls The Plum 360 is a large volume infuser capable of delivering fluids for a variety of therapies such as parenteral, ente…

March 25, 2016 · Medical device recalls Moderate risk Firm's investigation determined that the Proximal Occlusion Alarms observed in…

Hospira Inc. recalls Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 via…

March 23, 2016 · Drug & medication recalls Failed pH Specifications: Confirmed high out of specification (OOS) results for…

Hospira Inc. recalls Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 via…

March 23, 2016 · Drug & medication recalls High risk Presence of Particulate Matter: Confirmed customer complaint for the presence o…

Hospira Inc. recalls 8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest,…

March 18, 2016 · Drug & medication recalls High risk Presence of Particulate Matter: particulate matter identified as an insect in o…

Hospira Inc. recalls Quelicin (Succinylcholine Chloride) Injection, USP 200 mg. (20 mg/mL), 10 mL Multiple-dose vial, packaged in 25 Unit vi…

March 15, 2016 · Drug & medication recalls Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot numbe…

Hospira Inc. recalls Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 04…

March 8, 2016 · Drug & medication recalls Moderate risk Chemical Contamination: Potential for contamination of the products with an aro…

Hospira Inc. recalls Mannitol I.V., 20%, USP (20 g/ 100 mL), Packaged in 250 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 04…

March 8, 2016 · Drug & medication recalls Moderate risk Chemical Contamination: Potential for contamination of the products with an aro…

Hospira Inc. recalls Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 040…

March 8, 2016 · Drug & medication recalls Moderate risk Chemical Contamination: Potential for contamination of the products with an aro…

Hospira Inc. recalls Dextrose Injection, USP, 70%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 040…

March 8, 2016 · Drug & medication recalls Moderate risk Chemical Contamination: Potential for contamination of the products with an aro…

Hospira Inc. recalls Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045,…

March 8, 2016 · Drug & medication recalls Moderate risk Chemical Contamination: Potential for contamination of the products with an aro…

Hospira Inc. recalls Aminosyn-PF (amino acids) 7%, Sulfite-Free, 500 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0409-4178-…

March 8, 2016 · Drug & medication recalls Moderate risk Chemical Contamination: Potential for contamination of the products with an aro…

Hospira Inc. recalls Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container…

February 2, 2016 · Drug & medication recalls Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report o…

Magnesium Sulfate in Water for Injection recalled over labeling errors

January 5, 2016 · Drug & medication recalls High risk Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wr…

Hospira Inc. recalls The Symbiq infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manne…

December 22, 2015 · Medical device recalls Moderate risk Potential for the Symbiq pole clamp assemblies to be missing the rubber stop pa…

Hospira Inc. recalls Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL), LifeShield, 20 mL, Glass Abboject Syringe with male luer loc…

September 29, 2015 · Drug & medication recalls Failed Impurities/Degradation Specifications: Out of Specification(OOS) results…

Hospira, Inc. recalls 1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Fore…

August 25, 2015 · Drug & medication recalls Moderate risk Presence of Particulate Matter: particulate matter identified as iron oxide, wa…

Hospira Inc. recalls Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx…

August 20, 2015 · Drug & medication recalls Moderate risk Defective Container: There were customer complaints of cracked and leaking glas…

Hospira product recalled over sterility concerns

July 2, 2015 · Drug & medication recalls Moderate risk Lack of assurance of sterility: Potential channel leaks near the threaded vial…

Hospira Inc. recalls KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake For…

June 30, 2015 · Drug & medication recalls Moderate risk Crystallization; identified as calcium salt of Ketorolac

Hospira Inc. recalls KETOROLAC Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Fill Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Fore…

June 30, 2015 · Drug & medication recalls Moderate risk Crystallization; identified as calcium salt of Ketorolac

Hospira Inc. recalls Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospi…

May 19, 2015 · Drug & medication recalls Failed pH Specifications: 12 month stability testing

Hospira Inc. recalls Bupivacaine Hydrochloride Inj., USP, 0.5% (5 mg/mL), Preservative-Free, 30 mL Single Use Vials, Rx only. HOSPIRA, INC.,…

April 23, 2015 · Drug & medication recalls High risk Presence of Particulate Matter: Presence of free-floating and embedded iron oxi…

Hospira Inc. recalls Ketorolac Tromethamine Inj. USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL…

April 13, 2015 · Drug & medication recalls Moderate risk Crystallization

Hospira Inc. recalls Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL…

April 13, 2015 · Drug & medication recalls Moderate risk Crystallization

Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira Inc., Lake Forest, IL, 6…

April 7, 2015 · Drug & medication recalls Moderate risk Lack of Sterility Assurance: The product has the potential to leak at the admin…

LACTATED RINGER'S IRRIGATION recalled over sterility concerns

March 11, 2015 · Drug & medication recalls High risk Non-Sterility: Confirmed customer report of dark, fibrous particulates floating…

MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION recalled over labeling errors

March 6, 2015 · Drug & medication recalls High risk Labeling: Wrong Bar Code: There is a potential for some units to be mislabeled…

5% DEXTROSE Injection recalled over sterility concerns

March 5, 2015 · Drug & medication recalls Moderate risk Lack of Assurance of Sterility: there is a potential for solution to leak at th…

Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7…

March 5, 2015 · Drug & medication recalls High risk Presence of Particulate Matter: Confirmed finding of human hair floating in IV…

Hospira Inc. recalls KETOROLAC Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Fill Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Fore…

January 23, 2015 · Drug & medication recalls Moderate risk Crystallization

Hospira Inc. recalls KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake For…

January 23, 2015 · Drug & medication recalls Moderate risk Crystallization

Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02

January 20, 2015 · Drug & medication recalls High risk Presence of Particulate Matter; Hospira has identified the particulate as a hum…

Hospira Inc. recalls Propofol Injectable Emulsion, 1%, 200 mg/20 mL, (10mg/mL), 20 mL, Single patient infusion vial, Contains Benzyl Alcohol…

December 23, 2014 · Drug & medication recalls Moderate risk Presence of Particulate Matter: The firm received a complaint of an embedded pa…

Hospira product recalled over sterility concerns

December 22, 2014 · Drug & medication recalls Moderate risk Lack of Assurance of Sterility: The product has the potential for solution to l…

Hospira Inc. recalls MitoXANTRONE Injection, USP, (concentrate) 2 mg/mL, Rx Only. Hospira, Lake Forest, IL 60045, Product of Australia. Avai…

December 3, 2014 · Drug & medication recalls High risk Failed Stability Specifications: Product is subpotent and has out of specificat…

Hospira Inc. recalls 1% LIDOCAINE HCl Injection, USP, 10 mg/mL, 30 mL Single-dose, Preservative-Free glass vial (Twenty-five (25) units per…

October 16, 2014 · Drug & medication recalls High risk Presence of particulate matter: A returned customer sample was evaluated and fo…

Propofol Injectable Emulsion recalled over temperature-control failures

October 6, 2014 · Drug & medication recalls High risk Temperature Abuse: Products experienced uncontrolled temperature excursions dur…

Ketorolac Tromethamine Inj recalled over temperature-control failures

October 6, 2014 · Drug & medication recalls Moderate risk Temperature Abuse: Products experienced uncontrolled temperature excursions dur…

Vancomycin Hydrochloride for Injection recalled over temperature-control failures

October 6, 2014 · Drug & medication recalls Moderate risk Temperature Abuse: Products experienced uncontrolled temperature excursions dur…

Vancomycin Hydrochloride for Injection recalled over temperature-control failures

October 6, 2014 · Drug & medication recalls Moderate risk Temperature Abuse: Products experienced uncontrolled temperature excursions dur…

LACTATED RINGER'S and 5% DEXTROSE Injection USP recalled over sterility concerns

July 10, 2014 · Drug & medication recalls High risk Non-Sterility: Confirmed customer complaint of particulate matter floating with…

Hospira Inc. recalls The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environm…

July 2, 2014 · Medical device recalls High risk One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fai…

Hospira Inc. recalls The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environm…

July 2, 2014 · Medical device recalls High risk One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fai…

Hospira Inc. recalls The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environm…

July 2, 2014 · Medical device recalls High risk One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fai…

Hospira Inc. recalls The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environm…

July 2, 2014 · Medical device recalls High risk One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fai…

Hospira Inc. recalls The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environm…

July 2, 2014 · Medical device recalls High risk One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fai…

Hospira Inc. recalls Plum A+ Infusion System with Hospira MedNet List 20792-04-25, Pole Clamp Assembly Part Number 820-95443-008. A cassette…

June 11, 2014 · Medical device recalls Moderate risk Plum A+ infusion system pole clamp assemblies were discovered to be cracked. If…

Hospira Inc. recalls 1% LIDOCAINE HCl Injection, USP, Preservative-Free, 10 mg/mL, 30 mL Single-dose vials, packaged in 25-count cartons, Rx…

April 18, 2014 · Drug & medication recalls High risk Presence of Particulate Matter: Confirmed customer complaint that orange and bl…

Hospira Inc. recalls Hospira RECEPTAL LINERS: 1L(1000mL), 1.5L (1500mL), 2L (2000mL) 1) List Number 43056-01; 2) List Number 43023-01; 3) Li…

September 10, 2013 · Medical device recalls Moderate risk Hospira has become aware of customers using the incorrect size Receptal liners…

Hospira Inc. recalls Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers 43449-…

September 10, 2013 · Medical device recalls Moderate risk Hospira has become aware of customers using the incorrect size Receptal liners…

Hospira Inc. recalls *** 1) Product labeled in part: 19734-28; LIFESHIELD; LIFESHIELD LATEX-FREE PLUM SET, MICRODRIP,PP SOLUSET,FILTER, 3 CL…

September 9, 2013 · Medical device recalls Moderate risk Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV ad…

Hospira Inc. recalls *** 1) Product labeled in part: 19683-28; LIFESHIELD; MICRODRIP SOLUSET WITH 1.2 MICRON FILTER 150ML BURETTE PLUMSET, C…

September 9, 2013 · Medical device recalls Moderate risk Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV ad…

Hospira Inc. recalls *** 1) Product labeled in part: List No. 14212-28; LIFESHIELD; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, No…

September 9, 2013 · Medical device recalls Moderate risk Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV ad…

Hospira Inc. recalls *** 1) Product labeled in part: 14951-48; LIFESHIELD; PLUMSET WITH CONVERTIBLE PIERCING PIN, TWO INTEGRAL CLAVE PORTS A…

September 9, 2013 · Medical device recalls Moderate risk Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV ad…

Hospira Inc. recalls *** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, CLAVE Y-Site,…

September 9, 2013 · Medical device recalls Moderate risk Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV ad…

Hospira Inc. recalls The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through t…

March 8, 2013 · Medical device recalls Moderate risk Hospira has received reports of PCA pumps not detecting distal occlusions, one…

Hospira Inc. recalls The PCA 3 system cam be used in a wide range of clinical settings, including but not limited to: general floor, labor/d…

March 8, 2013 · Medical device recalls Moderate risk Hospira has received reports of PCA pumps not detecting distal occlusions, one…

Hospira Inc. recalls The LifeCare Pump Model 4200 PCA Infuser makes possible the practical implementation of patient-controlled analgesia. T…

March 8, 2013 · Medical device recalls Moderate risk Hospira has received reports of PCA pumps not detecting distal occlusions, one…

Hospira Inc. recalls LifeCare PCA infusion system with Hospira MedNet software allows clinicians to administer, or patients to self-administ…

March 8, 2013 · Medical device recalls Moderate risk Hospira has received reports of PCA pumps not detecting distal occlusions, one…

Hospira Inc. recalls LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administra…

March 8, 2013 · Medical device recalls Moderate risk Screw rotation error occurring when the pump detects a mismatch between the num…

Hospira Inc. recalls LifeCare PCA 3, PCA Serial List Number 12384 Allows for clinician administration or self-administration of analgesic me…

March 8, 2013 · Medical device recalls Moderate risk Screw rotation error occurring when the pump detects a mismatch between the num…

Hospira Inc. recalls The PCA 3 infusion pump allows clinicians, or patients, to (self) Administer analgesia safely and effectively within cl…

February 27, 2013 · Medical device recalls Moderate risk The infusion pump has a clear plastic door that, due to its design, allows for…

Hospira Inc. recalls The LifeCare PCA infusion system with Hospira MedNet software allows clinicians, or patients, to (self) Administer anal…

February 27, 2013 · Medical device recalls Moderate risk The infusion pump has a clear plastic door that, due to its design, allows for…

Hospira Inc. recalls Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of dru…

February 19, 2013 · Medical device recalls Moderate risk Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Exten…