FDAClass IIJuly 15, 2020

Cardinal Health NPWT Occlusion Detection Canister 300cc recall

Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic…

Why was Cardinal Health NPWT Occlusion Detection Canister 300cc recalled?

Canisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model Numbers: 48-4000, Lot numbers:201829015, 201923314, 201923316, 201923319, 20192347, 201923414, 201923410.

Product
Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic…
Recalling firm
Cardinal Health 200, LLC
Quantity
1960
Distribution
Worldwide distribution - US Nationwide distribution and the country of Canada.
Recall date
July 15, 2020
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls