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

Recall Z-0245-2022 — Ilizarov Wire Tensioner, Model 71070341, UDI (10)08033201842072(10)21HP02550(11)210831(21E434

U.S. FDA — Device Enforcement · Italy · 2021-06-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0245-2022
Date of alert
2021-06-17
Country / jurisdiction
Italy
Risk level
Class II
Risk type
recall
Brand
Medicalplastic S.R.L.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
71070341
Reported risk: Medicalplastic s.r.l. is conducting a voluntary field action to remove a group of Ilizarov Wire Tensioners due to a manufacturing error. An internal washer of the Ilizarov Wire Tensioner has been made in a wrong plastic material that could wear and break during the sterilization process in autoclave. Consequently this could cause malfunctioning of the tensioner.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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