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All product recalls associated with Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
There is a leakage issue associated with the tubing in the manifold of the instrument.
Lack of assurance of sterility. Bacterial contamination detected in some media fill units