Stryker recalls Hoffman LRF Wire Tensioner REF 4933-9-100 due to potential wire tension misalignment from a loose adjustment ring. Affected units include Lot #J43995 with UDI-DI 07613252611035.
The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.
Stryker is recalling a specific wire tensioner component for the Hoffmann LRF System because its adjustment ring might become loose, causing incorrect wire tension settings. This could lead to improper function of the system, though serious injury risks are not described in the recall.
The adjustment ring on the wire tensioner can become loose over time, which may cause the wire tension to be set incorrectly. This could result in the system not functioning as intended, but the recall does not mention risks of injury or damage to the user.
Users of the Hoffmann LRF System who purchased the Stryker Hoffman LRF Wire Tensioner REF 4933-9-100 with Lot #J43995 or UDI-DI 07613252611035 are affected. The risk is lowest for those using the system correctly without high tension demands.
Check for the model number REF 4933-9-100 on the product. Affected units have Lot #J43995 and UDI-DI 07613252611035.
Verify the model number REF 4933-9-100 and lot number J43995 on the product.
The recall states the adjustment ring may become loose, causing incorrect wire tension settings, but does not mention injury risks or damage to the user.
Check for model number REF 4933-9-100 with lot number J43995 and UDI-DI 07613252611035.
The recall does not specify a remedy, so no action is required beyond checking if your product matches the affected details.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2219-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2219-2024 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
