The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as…
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described…
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described…
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Understanding this recall history
This page summarizes recall records in which the official source identifies Waldemar Link GmbH & Co. KG (Mfg Site) as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.