Z-1719-2019 Class II Terminated
FDA device recall Z-1719-2019 was initiated by Centurion Medical Products Corporation on March 29, 2019 and is designated Class II. Reason for recall: Compromised seal on the sterile barrier pouch. The recall status is terminated (terminated May 8, 2020).
Recall Details
- Product Type
- Devices
- Report Date
- June 12, 2019
- Initiation Date
- March 29, 2019
- Termination Date
- May 8, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
Product Description
Sterile Nail Clipper Concave Edge (67710)
Reason for Recall
Compromised seal on the sterile barrier pouch.
Distribution Pattern
US nationwide distribution.
Code Information
Lot 2018120701, exp 2023-11-30