Waldemar Link recalls LINK MP Monoblock Hip Stems (Sizes 14-25mm) for potential increased removal force during surgery, which may prolong procedures or require surgical 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 hip stem trial instruments that may require more force to remove after impaction, potentially prolonging surgery or needing procedure changes. This affects patients with mobility-limiting conditions, hip fractures, or joint defects.
The hip stem may become impacted (stuck) during surgery, requiring more force to remove. This could lead to longer surgery times or necessary modifications to the procedure to avoid complications.
Patients with mobility-limiting conditions, hip fractures, or joint defects who use these trial hip stems are most at risk. The recall applies to specific sizes (14-25mm) manufactured for such patients.
Check for the item number 136-114/00 and UDI-DI 04026575182084 on the packaging. The recall covers sizes 14-25mm intended for patients with mobility issues, hip fractures, or joint defects.
Look for item number 136-114/00 and UDI-DI 04026575182084 on the packaging or label.
The LINK MP Monoblock hip stem may require more force to remove after becoming impacted, potentially prolonging surgery or needing procedure modifications.
Sizes 14-25mm, intended for patients with mobility-limiting conditions, hip fractures, or joint defects.
Check for item number 136-114/00 and UDI-DI 04026575182084 on the packaging or label.
We’ve drafted a message you can send Waldemar Link to request your refund or repair — edit it as you like.
Subject: Recall Z-2345-2023 — Waldemar Link Waldemar Link Hello, I own a Waldemar Link that is covered by recall Z-2345-2023 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.
