INTERTAN 1 — Class II medical device recall Z-1133-2022
Ongoing recall by Smith & Nephew Orthopaedics GmbH, reported 2022-06-01, distributed nationwide. Right nails were anodized, marked, and labelled as left nails and vice versa
| Recall number | Z-1133-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew Orthopaedics GmbH, Tuttlingen, Germany |
| Recall initiated | 2022-04-22 |
| Classified | 2022-05-25 |
| Reported by FDA | 2022-06-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 17 units |
| UPC / GTIN / UDI-DI | 00885556040027, 00885556131633 |
| Lot numbers | 21LT56988, 21LT56989, 71676628 |
Product
INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Reason for recall
Right nails were anodized, marked, and labelled as left nails and vice versa
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-1133-2022. 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.