Integra Universal Flexible Arm part number REF 1362275 — Class II medical device recall Z-0906-2022
Ongoing recall by Integra LifeSciences Corp., reported 2022-04-20, distributed nationwide. Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resu
| Recall number | Z-0906-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra LifeSciences Corp., Princeton, NJ, United States |
| Recall initiated | 2022-02-28 |
| Classified | 2022-04-11 |
| Reported by FDA | 2022-04-20 |
| Distributed | Nationwide (US) |
| Quantity | 54 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 10381780074670 |
| Lot numbers | AC2008, AC2009, AC2101, AC2103, AC2106, AC2109, AC2110 |
| Model numbers | 1362275 |
Product
Integra Universal Flexible Arm part number REF 1362275
Reason for recall
Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.
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-0906-2022. 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.