PHALINX — Class II medical device recall Z-1625-2015
Terminated recall by Wright Medical Technology, Inc., reported 2015-05-27, distributed nationwide. The term DORSAL was laser etched on the incorrect side on some of the angled handles.
| Recall number | Z-1625-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2015-04-16 |
| Classified | 2015-05-18 |
| Reported by FDA | 2015-05-27 |
| Terminated | 2018-10-18 |
| Distributed | Nationwide (US) |
| Quantity | 121 units |
| Lot numbers | 1344534 |
| Model numbers | 45304012 |
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012, CONTENTS 1 EACH, RX ONLY
Reason for recall
The term DORSAL was laser etched on the incorrect side on some of the angled handles.
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-1625-2015. 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.