FDA Medical Device Recalls (openFDA)
ConvaTec, Inc: ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1 dressing/immediate package, 5 packages/market unit.
- Recall number
- Z-1495-2024
- Recalling firm
- ConvaTec, Inc
- Product
- ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1 dressing/immediate package, 5 packages/market unit.
- Status
- Open, Classified
- Initiated
- 2024-02-27
- Posted
- 2024-04-08
- Terminated
- not on file
- Reason
- The product does not meet sterility assurance level.
- Root cause
- Under Investigation by firm
- Action
- The recalling firm issued letters dated Feb-2024 via email on 2/27/2024 listing all product and serial numbers that were distributed worldwide. The letter explained the issue and the associated hazard and potential risk to the end user. The addressee was instructed to immediately examine their inventory and quarantine the affected product. If the product was further distributed, the consignee was requested to identify their customers of the recall at once and notify them. The recall was to be conducted to the end-user level. The enclosed response form was to be returned within 30 calendar days of receipt of the letter. Once the response form has been returned, the recalling firm will provide the consignee with a Certificate of Destruction for completion and the affected product is then to be immediately destroyed. Once the Certificate of Destruction is returned, the consignee will be credited.
- Quantity
- 63 market units
- Distribution
- US Nationwide distribution in the states of CA, MO, NM, PA, TX, and WA.
- Lot, serial or model codes
- Order #403204 - Lot numbers 3J00675, 3J02320, 3J02332, 3L04811, and 4A00343.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- NAC
- Firm FEI
- 3011987967
- Firm city
- Greensboro
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28