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

Recall Z-1388-2024 — Epix Universal Clip Applier, REF: CA500, STERILEEO

U.S. FDA — Device Enforcement · United States · 2024-01-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1388-2024
Date of alert
2024-01-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Applied Medical Resources Corp
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00607915125318
Reported risk: Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.
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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