FDA Medical Device Recalls (openFDA)
Centurion Medical Products Corporation: Sterile Nail Nipper, Barrel Spring (I68400), Sterile
- Recall number
- Z-1720-2019
- Recalling firm
- Centurion Medical Products Corporation
- Product
- Sterile Nail Nipper, Barrel Spring (I68400), Sterile
- Status
- Terminated
- Initiated
- 2019-03-29
- Posted
- not on file
- Terminated
- 2020-05-08
- Reason
- Compromised seal on the sterile barrier pouch.
- Root cause
- Packaging
- Action
- On March 29, 2019, Centurion issued URGENT PRODUCT RECALL NOTICES to customers via courier service. Customers were advised to take the following actions: 1) Inspect stock and quarantine product 2) Discontinue use of product immediately 3) Complete and return the accountability record via fax to 517-546-3356 or via email to Lcarpenter@centurionmp.com
- Quantity
- not on file
- Distribution
- US nationwide distribution.
- Lot, serial or model codes
- Lot 2018121101, exp 2023-11-30
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- PWC
- Firm FEI
- 3008403546
- Firm city
- Williamston
- Firm state
- MI
- 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