FDA Device recall Z-1720-2019
Sterile Nail Nipper, Barrel Spring (I68400), Sterile
- FDA Device
- Class II
- terminated
- Published 2019-06-12
On 2019-06-12 the FDA classified a Class II recall of Sterile Nail Nipper, Barrel Spring (I68400), Sterile by Centurion Medical Products, citing compromised seal on the sterile barrier pouch.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1720-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-29 |
| Published | 2019-06-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Centurion Medical Products |
| Distribution | US |
Product
Sterile Nail Nipper, Barrel Spring (I68400), Sterile
Reason
Compromised seal on the sterile barrier pouch.
Identifiers
| code_info | Lot 2018121101, exp 2023-11-30 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1720-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.