Waldem:Link recalls LINK MP Monoblock Hip Stem Trial Size 23 for potential need for more force during removal, possibly prolonging surgery. Affected patients with mobility issues may need 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
Waldem:Link is recalling trial hip stems of size 23 for patients with mobility-limiting conditions. The stems may require more force to remove after impaction, which could prolong surgery or necessitate surgical changes.
The hip stem may become stuck during surgery, requiring more force to remove. This could extend the surgery time or require adjustments to the procedure, especially for patients with mobility issues.
Patients with mobility-limiting diseases, hip fractures, or joint defects who use this trial stem are affected. Those with limited mobility are at higher risk due to potential surgical complications.
Check for the item number 136-23/00 and lot numbers B922118, B933169, C005023, C211017, or C240048. The product is intended for patients with mobility-limiting conditions, hip fractures, or joint defects.
Verify the item number and lot numbers listed in the recall notice to confirm if your hip stem is affected.
The LINK MP Monoblock trial hip stem size 23 may require more force to remove after impaction, potentially prolonging surgery or needing surgical adjustments.
The recall notice does not specify a contact for assistance.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Waldem:Link to request your refund or repair — edit it as you like.
Subject: Recall Z-2354-2023 — Waldem:Link Waldem:Link Hello, I own a Waldem:Link that is covered by recall Z-2354-2023 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.
