AVID Medical Recalls
172 recalls on record · August 24, 2016 to August 12, 2026 · Medical Devices
Recalls by year
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24
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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.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls ROBOTIC URO/GYN PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls ROBOTIC PROSTATECTOMY PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls PARTIAL NEPHRECTOMY PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls PACK GENERAL ROBOTIC. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls MAJOR THORACOSCOPY BASIN. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls LAVH PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls LAPAROSCOPY PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls LAPAROSCOPIC PROSTATECTOMY. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls LAPAROSCOPIC GYN. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls LAP CHOLE PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls HVI CARDIAC ROBOT PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls GYN ROBOTIC PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls GYN LAPAROSCOPY PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls GS ENDOSCOPY PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls GENERAL ROBOTIC PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls GENERAL LAPAROSCOPY TRAY. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls GEN LAPAROSCOPY PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls DAVINCI UROLOGY. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls DAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls DA VINCI PACK URO/PROSTATE. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls CT DAVINCI. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls CARDIAC ROBOT PACK. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls LAPAROSCOPIC TRAY. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
May 21, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
Hazard: An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
May 21, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
Hazard: An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
May 21, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
Hazard: An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard ANGIO PACK - Medical convenience kits Model Number: WRNM047-05
Hazard: Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard PACEMAKER PK - Medical convenience kits Model Number: WKMC120-02
Hazard: Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard PACEMAKER TRAY - Medical convenience kits Model Number: VMPB0003-10
Hazard: Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions