Halyard Arthroscopy Pack recalled for mislabeled shelf label
The shelf label on a Halyard Arthroscopy Pack was printed as "Extremity" instead of "Arthroscopy Pack." The recall covers 17 kits, and the notice reports no injuries.
From the FDA notice · Read the official notice ↗ · All AVID Medical recalls
What to do
- Set aside any Halyard Arthroscopy Pack, Model/Catalog SAMM014-21, with Lot 1698318 and expiration date 12/3/2026 (UDI-DI 10809160515600).
- Contact AVID Medical, Inc. about the recall. The notice doesn't say how to get a replacement or refund.
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- Halyard ARTHROSCOPY PACK. Model/Catalog Number: SAMM014-21.
- Sold in
- Nationwide
- Made for
- All ages (0 months and older)
Details
- Units affected
- 17 kits
- Illnesses reported
- None reported
- Manufactured in
- 9000 Westmont Dr, Toano, Virginia, United States
- Classification
- Class II
- Recall number
- Z-0358-2027
In the FDA's words
- Description
- Halyard ARTHROSCOPY PACK. Model/Catalog Number: SAMM014-21. Shelf label of kit is mislabeled as "Extremity" instead of "Arthroscopy Pack." Model/Catalog Number: SAMM014-21. UDI-DI: 10809160515600. Lot Number: 1698318. Expiration Date: 12/3/2026. Distribution: US Nationwide distribution in the state of Texas. Affected quantity: 17 kits
- Hazard
- Shelf label of kit is mislabeled as "Extremity" instead of "Arthroscopy Pack."
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