AVID Medical, Inc.
102 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for AVID Medical, Inc. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2025-09-17FDA-DeviceClass IIHalyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit.
Potential for open header bag seals, compromising sterility.
- 2025-09-17FDA-DeviceClass IIHalyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Potential for open header bag seals, compromising sterility.
- 2025-08-13FDA-DeviceClass IIROBOTIC URO/GYN PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIROBOTIC PROSTATECTOMY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIPARTIAL NEPHRECTOMY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIPARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIPACK GENERAL ROBOTIC. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIMAJOR THORACOSCOPY BASIN. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IILAVH PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IILAPAROSCOPY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IILAPAROSCOPIC PROSTATECTOMY. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IILAPAROSCOPIC GYN. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IILAP CHOLE PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIHVI CARDIAC ROBOT PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIGYN ROBOTIC PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIGYN LAPAROSCOPY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIGS ENDOSCOPY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIGENERAL ROBOTIC PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIGENERAL LAPAROSCOPY TRAY. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIGEN LAPAROSCOPY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIDAVINCI UROLOGY. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIDAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IIDA VINCI PACK URO/PROSTATE. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IICT DAVINCI. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IICARDIAC ROBOT PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-08-13FDA-DeviceClass IILAPAROSCOPIC TRAY. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-05-21FDA-DeviceClass IIHalyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
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.
- 2025-05-21FDA-DeviceClass IIHalyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
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.
- 2025-05-21FDA-DeviceClass IIHalyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
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.
- 2024-11-20FDA-DeviceClass IIHalyard ANGIO PACK - Medical convenience kits Model Number: WRNM047-05
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
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