Waldemar Link recalls BiMobile UHMWPE Liner (ID-28mm/OD-50mm, Ref 184-260/02) due to potential incorrect part numbers in labeling that could lead to patient record errors. Affected patients should contact the manufacturer for details.
The internal labeling included with these implants may include incorrect part numbers and could result in these incorrect labels being added to patient records.
Waldemar Link is recalling BiMobile UHMWPE Liners with specific dimensions and reference numbers because their internal labels might have wrong part numbers. This could cause patient records to be misidentified, which is serious for medical safety.
The internal labels on these implants might have incorrect part numbers. If these wrong labels are added to patient records, it could lead to misidentification of patients during medical procedures, potentially causing treatment errors.
Patients who received the recalled BiMobile UHMWPE Liner (ID-28mm/OD-50mm, Reference Number 184-260/02) for mobility issues, fractures, or defects. Those with the specific lot number 1707121 are most at risk.
Check if your BiMobile UHMWPE Liner has ID-28mm/OD-50mm dimensions and Reference Number 184-260/02. The lot number 1707121 is also associated with this recall.
Reach out to Waldemar Link to confirm if your implant has the recalled reference number and lot number.
The internal labeling may include incorrect part numbers, which could lead to patient records being misidentified.
Contact Waldemar Link to check if your implant matches the recalled reference number and lot number 1707121.
The recall addresses potential patient misidentification, not direct injury risks. The hazard is low risk as it involves labeling errors rather than immediate physical harm.
We’ve drafted a message you can send Waldemar Link to request your refund or repair — edit it as you like.
Subject: Recall Z-0728-2019 — Waldemar Link Waldemar Link Hello, I own a Waldemar Link that is covered by recall Z-0728-2019 from Waldemar Link. 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.
