Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1234-2020 — Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref : A22020500

U.S. FDA — Device Enforcement · France · 2019-11-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1234-2020
Date of alert
2019-11-11
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
Medicrea International
Product category
device
Product type
Devices
Reported risk: Incompatible universal counter torque (A22020500) with the nut driver T30 (A22020220)
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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