AVID Medical, Inc. recalls Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
- Recall date
- March 31, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1742-2025
- FDA classification
- Class II
- Brand / firm
- AVID Medical, Inc.
- Sold / distributed
- US Nationwide distribution in the states of IL & LA.
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
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