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

Recall Z-0165-2023 — MEDLINE RADIOLOGY PROCEDURE PACK, REF DYNJ67150A. Convenience kit used in medical procedures.

U.S. FDA — Device Enforcement · United States · 2022-09-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0165-2023
Date of alert
2022-09-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10195327027278
Reported risk: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
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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