ConMed recalls certain KIT_INFINITY_BASE Custom Procedural Kits for possible lateral misalignment of tip guides, which may delay surgery or require alternative procedures.
Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may require another device or alternate surgical method to be used
ConMed is recalling specific custom procedural kits for knee surgery that might be misaligned, potentially causing delays or requiring alternative surgical methods. This affects medical professionals using the kits in knee ligament reconstruction procedures.
The tip guides in these kits may be misaligned laterally, which could reduce the accuracy of the guide system. This might lead to delays in surgery or necessitate using alternative devices or surgical approaches.
Medical professionals performing knee ligament reconstruction procedures in Italy using the recalled kits. Those most at risk are surgeons and surgical teams handling the specific kits with serial numbers 1, 2, or 3.
Check for kits labeled KIT_INFINITY_BASE Custom Procedural Kit with serial numbers 1, 2, or 3. These kits were sold in Italy for knee ligament reconstruction procedures.
Look for serial numbers 1, 2, or 3 on the kit packaging or labels.
The tip guides may be misaligned laterally, which could affect the accuracy of the guide system and cause delays in surgery or require alternative procedures.
Kits labeled KIT_INFINITY_BASE Custom Procedural Kit with serial numbers 1, 2, or 3 sold in Italy for knee ligament reconstruction procedures.
No. The recall is for potential misalignment that may cause delays or require alternative procedures, not an immediate safety hazard.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1499-2021 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-1499-2021 from ConMed. 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.
