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Terminated

Sterile Nail Nipper, Barrel Spring (I68400), Sterile

FDA Recall Z-1720-2019 · Posted None

Recalling FirmCenturion Medical Products Corporation
Recall StatusTerminated
Product CodePWC
Date Initiated2019-03-29
Date Terminated2020-05-08

Reason for Recall

Compromised seal on the sterile barrier pouch.

Firm 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 [email protected]

Root Cause

Packaging

Distribution Pattern

US nationwide distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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