Reported Jul 3, 2024 · Ongoing

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

Stryker GmbH

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Stryker GmbH · Bohnackerweg 1 · Selzach · N/A

Is this the product you have?

  • Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Lot codes and dates
    • Lot #J43995
    • UDI-DI 07613252611035
Amount recalled
39 devices

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:13 PM UTC

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