Waldemar Link recalls LINK MP Monoblock Hip Stem (Size 21) for potential surgery prolongation due to increased removal force. Affected patients with mobility issues may need procedure adjustments.
Increased force may be required to remove the LINK MP Monoblock trial hip stem (Sizes 14mm - 25mm),after impaction. Potential for prolongation of surgery or the surgical procedure may have to be modified due to this issue
Waldemar Link is recalling LINK MP Monoblock Hip Stem (Size 21) for patients with mobility-limiting conditions. The issue could require longer surgery or modifications to the procedure due to increased force needed to remove the hip stem.
The hip stem may require more force to remove after it becomes impacted. This could lead to longer surgery times or necessary procedure changes to avoid complications.
Patients with mobility-limiting diseases, hip fractures, or joint defects who have received the LINK MP Monoblock Hip Stem (Size 21) are affected. Those with recent hip surgery are most at risk.
Check for the item number 136-121/00 and UDI-DI 04026575182152 on the hip stem. Lot numbers B922120, B933167, C005021, and C211015 are also associated with this recall.
Look for item number 136-121/00 and UDI-DI 04026575182152 on the hip stem, or lot numbers B922120, B933167, C005021, or C211015.
No, the recall does not require immediate removal. Patients should check if they have the recalled item and follow the provided steps.
The hip stem may require more force to remove after it becomes impacted, which could prolong surgery or require procedure modifications.
Check for the item number 136-121/00 and UDI-DI 04026575182152 on the hip stem, or lot numbers B922120, B933167, C005021, or C211015. If you have the recalled item, contact Waldemar Link for further instructions.
We’ve drafted a message you can send Waldem: Link to request your refund or repair — edit it as you like.
Subject: Recall Z-2352-2023 — Waldem: Link Waldem: Link Hello, I own a Waldem: Link that is covered by recall Z-2352-2023 from Waldem: 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.
