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Cardinal Health 200, LLC recalls Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for
Recalled July 15, 2020 · FDA recall Z-2544-2020 · Cardinal Health 200
Hazard
Canisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device. · FDA Class II
Units
1960
Sold at
Worldwide distribution - US Nationwide distribution and the country of Canada.
Description
Canisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device.
Product
Cardinal Health NPWT Occlusion Detection Canister 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 PRO family of systems provides care in the acute, extended and home care settings.
Manufacturer(s)
Cardinal Health 200, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →