Panta Nail — Class II medical device recall Z-1539-2017
Terminated recall by Integra LifeSciences Corp., reported 2017-03-29, distributed nationwide. Voluntary recall/Removal of Panta and Panta XI Nails because there may be the potential that the internal and
| Recall number | Z-1539-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra LifeSciences Corp., Plainsboro, NJ, United States |
| Recall initiated | 2017-03-03 |
| Classified | 2017-03-23 |
| Reported by FDA | 2017-03-29 |
| Terminated | 2018-05-21 |
| Distributed | Nationwide (US) |
| Quantity | 4,449 units |
| Reason classes | sterility, packaging |
| Lot numbers | E2W1/1, EP14, EPG0/1, EPG0/2, EPG0/3, EPG0/4, EPG0/5, F0F1, F0WQ, F15L, F15L/1, F15M, F1ZQ, F1ZS, F27T, F27U, F27V, F33A, F33B, F33C, F33D, F3BN, F3BP, F3BQ, F3BR, F3H8, F3M9, F3MA, F3MB, F3MC, F3MD, F3Y5, F3Y6, F3Y7, F3Y8, F4H4, F4H5, F4H6, F4H7, F4H8 and 83 more |
| Model numbers | 500050ND, 500080ND, 500150ND, 500180ND, 500250ND, 500280ND, 500350ND, 500380ND, 510111ND, 51014ND, 510211ND, 510241ND, 510311ND, 510341ND |
Product
Panta Nail, Rx only, Sterile,
Reason for recall
Voluntary recall/Removal of Panta and Panta XI Nails because there may be the potential that the internal and external package seal does not provide the level of sterility intended.
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-1539-2017. 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.