Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1743-2025 — Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.

U.S. FDA — Device Enforcement · United States · 2025-03-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1743-2025
Date of alert
2025-03-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
AVID Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10809160211311
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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