TELEFLEX MEDICAL INC recalls

32 recalls on record · latest: April 11, 2022

Official U.S. recall history for TELEFLEX MEDICAL INC, compiled from official government records.

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Gibeck Humid-Vent 2S Flex DC recalled over sterility concerns

April 11, 2022 · Medical device recalls Moderate risk Reports received of torn corrugated breathing tubes.

Teleflex Flex tube recalled over sterility concerns

April 11, 2022 · Medical device recalls Moderate risk Reports received of torn corrugated breathing tubes.

TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-…

January 11, 2022 · Medical device recalls High risk The firm received reports indicating PTD tip separation during use.

TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containing components: PT-6570…

January 11, 2022 · Medical device recalls High risk The firm received reports indicating PTD tip separation during use.

TELEFLEX MEDICAL INC recalls 5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing components: PT-030…

January 11, 2022 · Medical device recalls High risk The firm received reports indicating PTD tip separation during use.

TELEFLEX MEDICAL INC recalls Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Percut…

January 11, 2022 · Medical device recalls High risk The firm received reports indicating PTD tip separation during use.

TELEFLEX MEDICAL INC recalls Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45509-S6, PT-45509-T The…

January 11, 2022 · Medical device recalls High risk The firm received reports indicating PTD tip separation during use.

TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65…

January 11, 2022 · Medical device recalls High risk The firm received reports indicating PTD tip separation during use.

TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-127…

January 11, 2022 · Medical device recalls High risk The firm received reports indicating PTD tip separation during use.

TELEFLEX MEDICAL INC recalls RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is…

February 18, 2021 · Medical device recalls Moderate risk Teleflex is voluntarily recalling the products referenced above due to customer…

PLEUR-EVAC Thoracic Catheters recalled over laceration hazard

February 12, 2021 · Medical device recalls Moderate risk Teleflex is recalling this product due to a lack of assurance of sterility.

TELEFLEX MEDICAL INC recalls Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical proced…

August 7, 2020 · Medical device recalls Moderate risk Potential sterility issue

TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device inten…

July 6, 2020 · Medical device recalls Moderate risk Breaking at the point of a welded joint

TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) - Product Usage: The laryngoscope is a device inten…

July 6, 2020 · Medical device recalls Moderate risk Breaking at the point of a welded joint

TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) - Product Usage: The laryngoscope is a device inte…

July 6, 2020 · Medical device recalls Moderate risk Breaking at the point of a welded joint

TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intende…

July 6, 2020 · Medical device recalls Moderate risk Breaking at the point of a welded joint

TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) - Product Usage: The laryngoscope is a device inten…

July 6, 2020 · Medical device recalls Moderate risk Breaking at the point of a welded joint

TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) - Product Usage: The laryngoscope is a device inten…

July 6, 2020 · Medical device recalls Moderate risk Breaking at the point of a welded joint

TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) - Product Usage: The laryngoscope is a device inten…

July 6, 2020 · Medical device recalls Moderate risk Breaking at the point of a welded joint

TELEFLEX MEDICAL INC recalls Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air and…

June 30, 2020 · Medical device recalls Moderate risk Potential for sterile packaging to be compromised¿

TELEFLEX MEDICAL INC recalls Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-8000I - Product Usage: CHEST DRAINAGE: To evacuate air and/or fl…

June 30, 2020 · Medical device recalls Moderate risk Potential for sterile packaging to be compromised¿

TELEFLEX MEDICAL INC recalls RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 10…

May 29, 2020 · Medical device recalls Moderate risk Teleflex is initiating a voluntary recall for the above-mentioned products due…

TELEFLEX MEDICAL INC recalls Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

January 13, 2020 · Medical device recalls Moderate risk There is a potential for the device packaging to become compromised; thus, the…

TELEFLEX MEDICAL INC recalls Teleflex Medical Disposable Aortic Punch, in the following sizes: a) 2.8 mm, REF DP-28K b) 3.6 mm, REF DP-36K c) 4.0 mm…

January 13, 2020 · Medical device recalls Moderate risk There is a potential for the device packaging to become compromised; thus, the…

TELEFLEX MEDICAL INC recalls Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System

January 9, 2020 · Medical device recalls Moderate risk The products are being recalled due to reports of breakage broke at the point o…

TELEFLEX MEDICAL INC recalls Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System

January 9, 2020 · Medical device recalls Moderate risk The products are being recalled due to reports of breakage broke at the point o…

TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit

December 13, 2019 · Medical device recalls High risk There is the potential for water to flood the column and enter the circuit unde…

TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Corrugated Humidification System, REF 2415, humidifier nebulizer kit

December 13, 2019 · Medical device recalls High risk There is the potential for water to flood the column and enter the circuit unde…

TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port, REF 2414, humidifier nebulizer kit

December 13, 2019 · Medical device recalls High risk There is the potential for water to flood the column and enter the circuit unde…

TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote Temperature Port, REF 2416, humidifier nebulizer kit

December 13, 2019 · Medical device recalls High risk There is the potential for water to flood the column and enter the circuit unde…

TELEFLEX MEDICAL INC recalls Sprotte Needle, REF 32115130C w/ Intro 22 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needles…

October 11, 2019 · Medical device recalls Moderate risk Teleflex received the attached Medical Device Recall Notice from Pajunk Medical…

TELEFLEX MEDICAL INC recalls Sprotte Needle, REF 33115131B w/ Intro 20 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needles…

October 11, 2019 · Medical device recalls Moderate risk Teleflex received the attached Medical Device Recall Notice from Pajunk Medical…