Waldemar Link GmbH & Co. KG (Mfg Site): Device Recall

Recall #Z-2411-2024 · 05/22/2024

Class II: Risk

Recall Details

Recall Number
Z-2411-2024
Classification
Class II
Product Type
Device
Recalling Firm
Waldemar Link GmbH & Co. KG (Mfg Site)
Status
Ongoing
Date Initiated
05/22/2024
Location
Norderstedt, Germany
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
114 units US; 2351 units OUS

Reason for Recall

Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique

Product Description

Endo Model SL Tibial Components 16-2817/02 Tibial Component, Small, W: 60mm 16-2817/05 Tibial Component, Medium, W: 65mm 16-2817/07 Tibial Component, Large, W: 75mm 16-2817/32 Tibial Component Modular, Small, W: 60mm 16-2817/35 Tibial Component Modular, Medium, W: 65mm 16-2817/37 Tibial Component Modular, Large, W: 75mm

Distribution Pattern

Nationwide Foreign: Algeria Argentina Australia Austria Belarus Belgium Brazil Bulgaria Canada China Colombia Czechia Denmark Ecuador Estonia Finland France Germany Greece Hungary India Indonesia Israel Italy Kenya Lithuania Luxembourg Mexico Netherlands Norway Peru Poland Romania Saudi Arabia Slovakia Slovenia Spain Sweden Switzerland Thailand T¿rkiye Ukraine United Arab Emirates United Kingdom Uruguay Vietnam

Other Recalls by Waldemar Link GmbH & Co. KG (Mfg Site)

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Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.