Wright Medical recalls DARCO Locking Bone Plate System due to incorrect manufacturing and distribution dates on labels. Affected units may have safety risks if used without proper date verification.
Product was labelled with the incorrect manufacturing and distribution dates.
Wright Medical is recalling their DARCO Locking Bone Plate System because the product was labeled with the wrong manufacturing and distribution dates. This could lead to confusion about when the product was made or distributed, potentially affecting safety if used without proper date verification.
The product was labeled with incorrect manufacturing and distribution dates. This could lead to confusion about when the product was made or distributed, potentially affecting safety if used without proper date verification. The hazard is low risk as it does not involve physical harm but rather labeling errors.
Orthopedic surgeons and medical professionals who use the DARCO Locking Bone Plate System for surgical procedures. Patients receiving this type of surgery are at risk if the incorrect dates cause confusion in the surgical process.
Check for the model number DCS282:126 and lot number 11012187061566009 on the product labels. The product was sold by Wright Medical Technology, Inc. and is used in orthopedic surgeries.
Verify the model number DCS2825126 and lot number 11012187061566009 on the product labels.
The DARCO Locking Bone Plate System was labeled with incorrect manufacturing and distribution dates.
Check for the model number DCS2825126 and lot number 11012187061566009 on the product labels.
Verify the model and lot numbers on the labels to confirm if the product is affected. No specific action is required beyond checking the labels.
We’ve drafted a message you can send Wright Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0679-2022 — Wright Medical Wright Medical Hello, I own a Wright Medical that is covered by recall Z-0679-2022 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.
