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

Recall Z-2543-2020 — Cardinal Health NPWT Canister with Gel 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic, acute, traumatic, sub-acute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts. The Cardinal Health NPWT PR

U.S. FDA — Device Enforcement · United States · 2020-06-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2543-2020
Date of alert
2020-06-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
201921913
Reported risk: Canisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device.
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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