FDAClass IIIOctober 5, 2022

3m Systagenix/kci Kerracel Ag Dressing recall

3M SYSTAGENIX/KCI KerraCel Ag DRESSING, WOUND KERRACEL AG 4X5 (10/CT 10CT/CS) Catalog #CWL1158

Why was 3m Systagenix/kci Kerracel Ag Dressing recalled?

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

GTIN: 05060077233539 EA; 05060077233546 CA; 05060077233553 CS

Product
3M SYSTAGENIX/KCI KerraCel Ag DRESSING, WOUND KERRACEL AG 4X5 (10/CT 10CT/CS) Catalog #CWL1158
Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
Quantity
16.9 ct
Distribution
US Nationwide distribution.
Recall date
October 5, 2022
Classification
Class III
Status
Ongoing
Agency
FDA (device)
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