Wright Medical recalls Stryker CLAW II ORTHOLOC 3DSi plates with incorrect product in packaging. Affected units have specific model and lot numbers. No action needed as the hazard is packaging error, not a product defect.
The incorrect product is contained in the packaging.
Wright Medical is recalling a specific Stryker CLAW II ORTHOLOC 3DSi plate model due to an incorrect product being included in the packaging. This does not pose a safety risk to users as it's a packaging error, not a defect in the product itself.
The recall is for an incorrect product being included in the packaging, not a defect in the actual plate. This means the plate itself is safe for use but the packaging contains the wrong item. There is no risk of injury or malfunction from the plate itself.
Orthopedic surgeons and medical facilities that received the specific Stryker CLAW II ORTHOLOC 3DSi plate model with lot #1642103. Patients using this plate are not at risk as the issue is packaging-related.
Check for the model 'Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430' and lot number #1642103 on the packaging. This specific combination is affected by the recall.
Check the model number and lot number on the packaging to confirm if it matches the recalled items.
No, the recall is for an incorrect product in the packaging, not a defect in the plate itself. The product is safe for use.
No action is needed as the hazard is a packaging error, not a safety issue. The product is safe for use.
No action is required. The recall does not affect the safety of the product; it's a packaging error.
We’ve drafted a message you can send Wright Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0392-2022 — Wright Medical Wright Medical Hello, I own a Wright Medical that is covered by recall Z-0392-2022 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.
