Zimmer Biomet recalls 2.0MM Ball Nose Guide Wire with Item Nos. 281017006 due to elevated bacterial endotoxin and debris from cleaning issues. Affected units may pose infection risks during orthopedic procedures.
Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
Zimmer Biomet is recalling 2.0MM Ball Nose Guide Wire with specific item numbers because cleaning doesn't remove all bacterial endotoxins and debris. This could lead to infections during orthopedic surgeries if the device isn't properly cleaned.
The devices contain elevated levels of bacterial endotoxins and debris because the cleaning process doesn't fully remove contaminants. This could lead to infections during surgical procedures if the instruments aren't properly sterilized.
Orthopedic surgeons and medical professionals who use these devices for implanting orthopedic devices. Patients undergoing surgery with these instruments may be at risk of infection.
Check for item numbers listed in the recall (e.g., 281017006) on the device packaging or labels. The product is used for orthopedic implant procedures and was sold in specific lots.
Look for item numbers on the device packaging or labels to confirm if it's affected.
The recall states that elevated bacterial endotoxin and debris remain due to cleaning issues, so it's not safe for use without proper cleaning.
Check for item numbers listed in the recall (e.g., 281017006) on the device packaging or labels.
The recall doesn't specify a remedy, so contact Zimmer Biomet directly for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0531-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0531-2020 from Zimmer Biomet. 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.
