Waldemar Link recalls LINK MP Monoblock Hip Stem trial instruments (Size 20) for patients with mobility issues. Increased force may prolong surgery due to impaction risks.
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 trial hip stem instruments for patients with mobility-limiting conditions. These instruments may require more force to remove after impaction, potentially prolonging surgery or needing procedure changes.
The trial hip stem instruments may become impacted (stuck) during surgery, requiring more force to remove. This can prolong the surgical procedure or necessitate modifications to the surgery.
Patients with mobility-limiting diseases, hip fractures, or joint defects who use these trial hip stem instruments. Those with specific size 20 instruments are most at risk.
Check for the item number 136-120/00 and UDI-DI 04026575182145 on the instrument. Lot numbers B922121, B933166, C005012, and C211014 are also associated with this recall.
Verify the item number 136-120/00 and UDI-DI 04026575182145 on the instrument.
The trial hip stem instruments may require more force to remove after impaction, potentially prolonging surgery or needing procedure changes.
Patients with mobility-limiting diseases, hip fractures, or joint defects who use these trial hip stem instruments (Size 20).
Lot numbers B922121, B933166, C005012, and C211014.
We’ve drafted a message you can send Waldemar Link to request your refund or repair — edit it as you like.
Subject: Recall Z-2351-2023 — Waldemar Link Waldemar Link Hello, I own a Waldemar Link that is covered by recall Z-2351-2023 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.
