AVID Medical, Inc.
38 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.
- 2026-02-18FDA-DeviceClass IIHalyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
Tyvek bag seal issue which may compromise sterility of the kit.
- 2026-01-14FDA-DeviceClass IHalyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceClass IHalyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceClass IHalyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
Devices are not suitable for organ transplant.
- 2025-12-24FDA-DeviceClass IIHalyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.
Potential for incomplete seal on header bag.
- 2025-12-24FDA-DeviceClass IIHalyard, MAJOR PACK. Catalog Number: JEMJ10-01.
Potential for incomplete seal on header bag.
- 2025-12-24FDA-DeviceClass IIHalyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Potential for incomplete seal on header bag.
- 2025-12-24FDA-DeviceClass IIHalyard, EP LAB PK. Catalog Number: ESJH009-03.
Potential for incomplete seal on header bag.
- 2025-12-24FDA-DeviceClass IIHalyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.
Potential for incomplete seal on header bag.
- 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.
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