Natus Medical Incorporated recalls

15 recalls on record · latest: November 28, 2023

Official U.S. recall history for Natus Medical Incorporated, compiled from official government records.

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Natus Medical Incorporated recalls EDS 3 CSF External Drainage System, REF: NT821731C, STERILEEO, Rx only

November 28, 2023 · Medical device recalls Moderate risk Sterility assurance cannot be guaranteed for external drainage systems due to i…

Natus Medical Incorporated recalls External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only

November 28, 2023 · Medical device recalls Moderate risk Sterility assurance cannot be guaranteed for external drainage systems due to i…

Natus Medical Incorporated recalls The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set…

November 18, 2022 · Medical device recalls Moderate risk Due to Cranial Access Kits containing recalled sterile surgical drapes. The ste…

Natus Medical Incorporated recalls The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of re…

May 22, 2017 · Medical device recalls Moderate risk Olympic Pasteurmatic 3000/3500 Systems are recalled because they do not fully m…

Natus Medical Incorporated recalls Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between 2003 and 2008. Catalog Part Number 010066. To…

April 3, 2017 · Medical device recalls Moderate risk The second generation neoBLUE 2 lights with a black band, sold from 2003 to 200…

Natus Medical Incorporated recalls Natus neoBLUE blanket LED Phototherapy system, neonatal phototherapy. Used to provide treatment for neonatal Hyperbilir…

October 28, 2016 · Medical device recalls Moderate risk neoBLUE blanket LED Phototherapy System distributed since release of the produc…

Updated Natus neoBLUE blanket LED Phototherapy Systems recalled over fire hazard

September 16, 2016 · Medical device recalls Moderate risk The firm sent the Technical Bulletin to consignees who received the reliability…

Natus Medical Incorporated recalls The Medix NatalCare LX Intensive Care Incubator. Neonatal incubator. Item numbers: DMNCLX1; KITNC-STLX0003; KITNC-STLX0…

August 25, 2016 · Medical device recalls Moderate risk NatalCare LX incubators may have a defective base where the weld holding the wh…

Natus Medical Incorporated recalls Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model 44. Filter Catalogue Part Number: 54343, 54344, and…

April 22, 2016 · Medical device recalls Moderate risk The replacement HEPA Filters have been manufactured with sealant that may not b…

Natus Medical Incorporated recalls Natus neoBLUE Phototherapy system, Catalogue Part Number: 010066. Top Assembly Part Numbers: 001103, 001314, 002110, 04…

April 11, 2016 · Medical device recalls Moderate risk The firm is adding the warning statement to the Instruction for Use for the neo…

Natus Medical Incorporated recalls Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator.

January 8, 2016 · Medical device recalls Moderate risk NatalCare LX Incubators were manufactured using a defective oval port hinge ass…

Natus Medical Incorporated recalls Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy, Catalogue Part Number: 010066; Top Assembly Part Number:…

August 5, 2015 · Medical device recalls Moderate risk The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3 wer…

Natus Medical Incorporated recalls Natus neoBLUE blanket LED Phototherapy system which includes the following items: 006224 neoBLUE blanket LED Photothera…

March 16, 2015 · Medical device recalls Moderate risk neoBLUE blanket LED Phototherapy System is recalled because Natus has received…

Natus Medical Incorporated recalls EPWorks software used in the Protektor 32 Product Usage: Uses electroencephalography (EEG), evoked potentials (EP), ele…

January 2, 2015 · Medical device recalls Moderate risk Software error occurs when using remote monitoring; if the remote user tries to…

Natus Medical product recalled over laceration hazard

January 2, 2015 · Medical device recalls Moderate risk Software error occurs when using remote monitoring; if the remote user tries to…