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

Recall Z-1723-2026 — Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596

U.S. FDA — Device Enforcement · United States · 2026-02-27 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1723-2026
Date of alert
2026-02-27
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Medline Industries, LP
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10195327656119
Reported risk: Medline Industries, LP has identified through post-market surveillance a potential risk of the 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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