Home / Recalls / Medical Devices
Stryker GmbH recalls Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Recalled July 3, 2024 · FDA recall Z-2219-2024 · Stryker
Hazard
The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly. · FDA Class II
Units
39 devices
Sold at
Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, KY, MA, MI, NE, NJ, OH, OR, and TX. The countries of Germany, Japan, Netherlands, and United Kingdom.
Description
The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.
Product
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Manufacturer(s)
Stryker GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →