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

Recall Z-2695-2024 — LINER, SOFT, SUCTION CANISTER, 1500CC, REF OR929K

U.S. FDA — Device Enforcement · United States · 2024-03-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2695-2024
Date of alert
2024-03-22
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)
40888277276209
Reported risk: A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
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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