MicroPort Orthoped: Size 7 left knee tibial bases (lot 1916715) were recalled due to incorrect product packaging during surgery. Affected patients should contact the manufacturer for details.
One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging.
MicroPort Orthopedics recalled specific size 7 left knee tibial bases (lot 1916715) because they were found in the wrong packaging during surgery. This could lead to incorrect surgical implants if used.
The recall involves a confirmed incident where the wrong product (size 7) was found in the packaging of a size 2 tibial base during surgery. This could lead to incorrect implant placement if the wrong size is used in the procedure.
Patients who received the recalled size 7 left tibial bases (lot 1916715) during surgery are affected. Surgeons and surgical teams using these specific implants are at highest risk.
Check for the product name 'EVOLUTION MP Tibial Bases, Size 7 LEFT' with reference number ETPKN7SL and lot number 1916715. This was used in specific surgical procedures.
Reach out to MicroPort Orthopedics for details about your specific implant and next steps.
The recall was triggered by a confirmed incident where the wrong product (size 7) was found in the packaging of a size 2 tibial base during surgery.
The official notice does not specify injury risks beyond the incorrect product placement during surgery.
Check for the product name 'EVOLUTION MP Tibial Bases, Size 7 LEFT' with reference number ETPKN7SL and lot number 1916715.
We’ve drafted a message you can send MicroPort Orthopedics to request your refund or repair — edit it as you like.
Subject: Recall Z-0276-2023 — MicroPort Orthopedics MicroPort Orthopedics Hello, I own a MicroPort Orthopedics that is covered by recall Z-0276-2023 from MicroPort Orthopedics. 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.
