FDA Device recall Z-1234-2020
Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref : A22020500
- FDA Device
- Class II
- terminated
- Published 2020-02-26
On 2020-02-26 the FDA classified a Class II recall of Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref : A22020500 by Medicrea International, citing incompatible universal counter torque (A22020500) with the nut driver T30 (A22020220).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1234-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-11-11 |
| Published | 2020-02-26 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medicrea International |
| Distribution | CA, FL |
Product
Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref : A22020500
Reason
Incompatible universal counter torque (A22020500) with the nut driver T30 (A22020220)
Identifiers
| code_info | Lot Number:19H0108 Exp.Date: 19/08/2029 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1234-2020%22
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