AVID Medical, Inc. recalls Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containi
See all recalls from AVID Medical, Inc. →Recalled Product
Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
Hazard / Issue
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI: 10809160372357, Lot No.: 1669869, Expiration Date: 4/30/2027
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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