Home / Brands / Baxter Healthcare
Baxter Healthcare Recalls
556 recalls on record · June 20, 2012 to August 19, 2026 · Drugs, Medical Devices
Recalls by year
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 24, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Low Weight-Low Volume Blood Transport System for Hemodialysis Blood Set, product code 114435 - Product
Hazard: complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
February 24, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Low Volume Blood Transport System for Hemodialysis Blood Set, product code 114434 - Product Usage: inte
Hazard: complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
February 24, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Blood Transport System for Hemodialysis Blood Set, product code 109536 - Product Usage: intended for si
Hazard: complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
February 24, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Blood Transport System for Hemodialysis Blood Set, product code 106289 - Product Usage: intended for si
Hazard: complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
February 24, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Single Needle Conversion Kit, product code 101290 - Product Usage: intended for single use in a hemodia
Hazard: complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
February 24, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Blood Set Prime Line, product code 101025 - Product Usage: intended for single use in a hemodialysis tr
Hazard: complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
February 17, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, Neutral Fluid Displac
Hazard: There were customer reports of separation between the tubing and Male Luer Lock Adaptor.
February 10, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable d
Hazard: Potential for the battery to lose its ability to be recharged.
January 20, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal p
Hazard: VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.
January 13, 2021Medical DevicesFDA
Baxter Healthcare Corporation recalls MiniCap Extended Life PD Transfer Set
Hazard: Potential for no-flow and leaks under the twist clamp.
December 30, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software - Product Usage: intended to be used for the controlled
Hazard: There is a potential software error during programming.
December 30, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) - Product Usage: intended to be used for the co
Hazard: There is a potential software error during programming.
December 30, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) - Product Usage: intended to be used for the co
Hazard: There is a potential software error during programming.
December 30, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) - Product Usage: intended to be used for the co
Hazard: There is a potential software error during programming.
November 18, 2020DrugsFDA
Baxter Healthcare Corporation recalls Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% (15 mg/2 mL) 10 x 2 mL single-dose ampules, Rx o
Hazard: Presence of particulate matter in solution - black and transparent particles
October 28, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Spectrum IQ Infusion System with Dose IQ Safety Software
Hazard: Baxter is updating the device IFU for safety communication regarding cleaning practices.
October 28, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)
Hazard: Baxter is updating the device IFU for safety communication regarding cleaning practices.
October 28, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)
Hazard: Baxter is updating the device IFU for safety communication regarding cleaning practices.
October 28, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)
Hazard: Baxter is updating the device IFU for safety communication regarding cleaning practices.
July 8, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Flow Coupler Monitor, GEM, Global Excellence Microsurgery, Rx Only
Hazard: A firmware issue may cause the GEM1020M-2 Flow Coupler Monitor to intermittently shut down when a WiFi connection is not established.
June 10, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Low Weight-Low Volume Blood Transport System for Hemodialysis Blood Set - Product Usage: is intended fo
Hazard: Potential disconnection of tubing set.
June 10, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Low Volume Blood Transport System for Hemodialysis Blood Set - Product Usage: is intended for single us
Hazard: Potential disconnection of tubing set.
June 10, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Blood Transport System for Hemodialysis Blood Set - Product Usage: is intended for single use in a hemo
Hazard: Potential disconnection of tubing set.
June 10, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Gambro Cartridge Blood Set Prime Line - Product Usage: is intended for single use in a hemodialysis treatment using Dial
Hazard: Potential disconnection of tubing set.
May 27, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Prismaflex Control Unit
Hazard: Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed.
May 6, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Prismaflex System, Prismaflex Control Unit
Hazard: Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
May 6, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Prismaflex System, Prismaflex Control Unit
Hazard: Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
May 6, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Prismaflex System, Prismaflex Control Unit
Hazard: Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
May 6, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Prismaflex System, Prismaflex Control Unit
Hazard: Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
May 6, 2020Medical DevicesFDA
Baxter Healthcare Corporation recalls Prismaflex System, Prismaflex Control Unit
Hazard: Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.