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

Recall Z-2356-2023 — LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 25 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-25/00

U.S. FDA — Device Enforcement · Germany · 2023-07-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2356-2023
Date of alert
2023-07-03
Country / jurisdiction
Germany
Risk level
Class II
Risk type
recall
Brand
Waldemar Link GmbH & Co. KG (Mfg Site)
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04026575182190
Reported risk: Increased force may be required to remove the LINK MP Monoblock trial hip stem (Sizes 14mm - 25mm),after impaction. Potential for prolongation of surgery or the surgical procedure may have to be modified due to this issue
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.