Recall Z-2219-2024— Stryker GmbH
Class II · Ongoing
Class II FDA medical device recall by Stryker GmbH, initiated 2024-05-09. FDA's recall record names no specific 510(k) clearance for this event. Product: Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.. Reason: The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly..
- Recalling firm
- Stryker GmbH
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-05-09
- Firm location
- Selzach, Switzerland
Product description
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Reason for recall
The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.
Data sourced from openFDA. This site is unofficial and independent of the FDA.