Recall Z-1720-2019— Centurion Medical Products Corporation
Class II · Terminated
Class II FDA medical device recall by Centurion Medical Products Corporation, initiated 2019-03-29, terminated 2020-05-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Sterile Nail Nipper, Barrel Spring (I68400), Sterile. Reason: Compromised seal on the sterile barrier pouch..
- Recalling firm
- Centurion Medical Products Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-03-29
- Terminated
- 2020-05-08
- Firm location
- Williamston, MI, United States
Product description
Sterile Nail Nipper, Barrel Spring (I68400), Sterile
Reason for recall
Compromised seal on the sterile barrier pouch.
Data sourced from openFDA. This site is unofficial and independent of the FDA.