Class II

Medical Device Recall: Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.

Stryker GmbH · May 9, 2024

Reason for Recall

The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.

Distribution

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.

States Affected

NATIONWIDE

Quantity Affected

39 devices

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2219-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Stryker GmbH Medical Device Recall: Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System. | SafeCheck