Allofix Insertion Kit — Class II medical device recall Z-2075-2015
Terminated recall by Musculoskeletal Transplant Foundation, Inc., reported 2015-07-22, distributed nationwide. Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are la
| Recall number | Z-2075-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc., Edison, NJ, United States |
| Recall initiated | 2015-05-27 |
| Classified | 2015-07-15 |
| Reported by FDA | 2015-07-22 |
| Terminated | 2017-05-08 |
| Distributed | Nationwide (US) |
| Quantity | 117 units |
| Reason classes | labeling |
| Serial numbers | 906912041001 |
| Expiration dates | 2017-03-01 |
Product
Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orthopedic surgeon and are intended to be used in conjunction with the associated allograft. This kit is for single use only.
Reason for recall
Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it may contain a 2.4 mm diameter drill.
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-2075-2015. 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.