Sterile Low Profile Screw — Class II medical device recall Z-2733-2020
Terminated recall by Arthrex, Inc., reported 2020-08-05. Screws provided in packaging are 5mm shorter than intended
| Recall number | Z-2733-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arthrex, Inc., Naples, FL, United States |
| Recall initiated | 2020-06-24 |
| Classified | 2020-07-29 |
| Reported by FDA | 2020-08-05 |
| Terminated | 2021-02-16 |
| Countries outside the US | DK, GB, JP, NL, SE |
| Quantity | 28 units |
| UPC / GTIN / UDI-DI | 00888867056411 |
| Lot numbers | 10706233 |
| Model numbers | AR-8967-2865S |
Product
Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions.
Reason for recall
Screws provided in packaging are 5mm shorter than 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-2733-2020. 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.