Class II — ulrich medical USA Inc
| Recalling firm | ULRICH MEDICAL USA, INC. |
|---|---|
| Registered facility | ULRICH MEDICAL USA, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Certain Torque Limiting Handles in the field are beyond their 3 year calibration life. |
| Product | ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the final tightening of set screws in a spinal implant construct. |
| Quantity | 25 |
| Distribution | AZ, IL, LA, MI, MO, NV, OH, PA, TN, and TX. |
| Initiated | 2019-03-08 |
| Classified | 2019-04-11 |
| Terminated | 2020-07-10 |
| Recall number | Z-1126-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — ulrich medical USA Inc (Z-1126-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82497/
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