Breg Recalls
13 recalls on record · February 20, 2013 to November 15, 2023 · Medical Devices
Recalls by year
13
14
17
23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 15, 2023Medical DevicesFDA
Breg Inc recalls BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.
Hazard: Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
May 10, 2017Medical DevicesFDA
Breg Inc recalls If Hip, Sterile Polar Dressing P/N 10680 Product Usage: These products are sterile dressings used as an insulation b
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
May 10, 2017Medical DevicesFDA
Breg Inc recalls Dressing Back, P/N 09810 Product Usage: These products are sterile dressings used as an insulation barrier between t
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
May 10, 2017Medical DevicesFDA
Breg Inc recalls Dressing Shldr XL, P/N 04918 Product Usage: These products are sterile dressings used as an insulation barrier betwe
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
May 10, 2017Medical DevicesFDA
Breg Inc recalls Dressing Shldr, P/N 04908 Product Usage: These products are sterile dressings used as an insulation barrier between
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
May 10, 2017Medical DevicesFDA
Breg Inc recalls Dressing, Knee L/XL, P/N 04708 Product Usage: These products are sterile dressings used as an insulation barrier bet
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
May 10, 2017Medical DevicesFDA
Breg Inc recalls Dressing Rect L, P/N 02428 Product Usage: These products are sterile dressings used as an insulation barrier between
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
May 10, 2017Medical DevicesFDA
Breg Inc recalls Dressing M/U XL, P/N 02344 Product Usage: These products are sterile dressings used as an insulation barrier between
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
May 10, 2017Medical DevicesFDA
Breg Inc recalls Dressing Knee/Shldr, P/N 02328 Product Usage: These products are sterile dressings used as an insulation barrier bet
Hazard: They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.
April 16, 2014Medical DevicesFDA
Breg Inc recalls K-Lite Knee 2 Stays with Visco, Model No. 122015. Product Usage: The product is intended to provide flexible knee su
Hazard: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2 Stays with Visco because they contain latex but were not labeled with the required caution label.
April 16, 2014Medical DevicesFDA
Breg Inc recalls Economy Elastic Knee Sleeve Open, Model No. 121414 and 121415. Product Usage: The product is intended to provide flex
Hazard: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2 Stays with Visco because they contain latex but were not labeled with the required caution label.
February 20, 2013Medical DevicesFDA
Breg Inc recalls BREG Sterile Polar Pads; 02356 Rev M, PAD M/U XL STER, Mfg.Date: 112012. Model #s: 02510, 09901, 02330, 02350, 02490, 02
Hazard: The recall was initiated because Breg has determined that some Sterile Polar Pads products manufactured from January 2010 to October 2012 may have sustained damage to the product packaging which may compromise product sterility assurance.
February 20, 2013Medical DevicesFDA
Breg Inc recalls BREG Cold Therapy Combination Units containing Sterile Polar Pads. 02356 Rev M, PAD M/U XL STER, Mfg.Date: 112012. Mode
Hazard: The recall was initiated because Breg has determined that some Sterile Polar Pads products manufactured from January 2010 to October 2012 may have sustained damage to the product packaging which may compromise product sterility assurance.