T7 Driver Solid AO — Class II medical device recall Z-1303-2019
Terminated recall by Zimmer Biomet, Inc., reported 2019-05-15, distributed nationwide. There is a potential of fracture, bending or shearing of the driver.
| Recall number | Z-1303-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-03-28 |
| Classified | 2019-05-09 |
| Reported by FDA | 2019-05-15 |
| Terminated | 2020-06-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CR, MY, NL, SG |
| Quantity | 1,924 |
| Reason classes | device malfunction |
| Lot numbers | 13421A, 13811A, 14042B, 14048B, 14140A, 14194B, 14343A, 14392A, 14393A, 14394A, 14518A, 14601A, 14827B, 14895C, 15015B, 15167B, 15257A, 15392A |
| Model numbers | 110018541 |
Product
T7 Driver Solid AO (Part Number 110018541) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) or bone reconstruction (osteotomy) of the mid-foot bones, metatarsal and phalanges of the foot or the phalanges, metacarpals and carpals of the hand. In the foot, these include procedures to correct Hallux Valgus (bunions), Hallux Varus and Hallux Rigidus, Hammer toe, Claw toe and Mallet toe.
Reason for recall
There is a potential of fracture, bending or shearing of the driver.
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-1303-2019. 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.