Wright Medical recalls Stryker DARCO Screw (REF DC2825016) due to incorrect product in packaging. Affected units may contain wrong item; contact for details.
The incorrect product is contained in the packaging.
Wright Medical is recalling a specific Stryker DARCO Screw model because it was incorrectly packaged. This means some buyers might have received the wrong screw, which could lead to improper use in medical procedures.
The recall states that the incorrect product is in the packaging. This means the wrong screw could be used in medical procedures, potentially causing improper fixation or complications during surgery.
Medical professionals and facilities that purchased the Stryker DARCO Screw (REF DC2825016) with lot number 1643355 are likely affected. Those using the product for surgical procedures are at the highest risk.
Check for the product name 'Stryker DARCO Screw, Locking, Ti6A14V' with reference number DC2825016 and lot number 1643355 on the packaging.
Verify the product name, reference number DC2825016, and lot number 1643355 on the packaging to confirm if it's the recalled item.
The recall states the incorrect product is in the packaging, but it does not specify that the product causes injury if used. The hazard is about receiving the wrong item, not the product's function.
Look for the product name 'Stryker DARCO Screw, Locking, Ti6A14V' with reference number DC2825016 and lot number 1643355 on the packaging.
The recall does not provide a remedy, so no action is required beyond checking the packaging to confirm if it's the recalled item.
We’ve drafted a message you can send Wright Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0393-2022 — Wright Medical Wright Medical Hello, I own a Wright Medical that is covered by recall Z-0393-2022 from Wright Medical. 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.
