Sterile Nail Nipper — Class II medical device recall Z-1720-2019
Terminated recall by Centurion Medical Products Corporation, reported 2019-06-12, distributed nationwide. Compromised seal on the sterile barrier pouch.
| Recall number | Z-1720-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2019-03-29 |
| Classified | 2019-06-04 |
| Reported by FDA | 2019-06-12 |
| Terminated | 2020-05-08 |
| Distributed | Nationwide (US) |
| Reason classes | sterility, packaging |
| Lot numbers | 2018121101 |
| Expiration dates | 2023-11-30 |
Product
Sterile Nail Nipper, Barrel Spring (I68400), Sterile
Reason for recall
Compromised seal on the sterile barrier pouch.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1720-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.