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

Recall Z-1970-2026 — Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.

U.S. FDA — Device Enforcement · United States · 2026-03-13 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1970-2026
Date of alert
2026-03-13
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
AVID Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10809160377314
Reported risk: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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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