Covidien recalls 15x10cm polyester mesh for inguinal hernia repair due to incorrect side labeling. Using right-side mesh for left-side repairs risks hernia recurrence. Affected items have specific item code and lot numbers.
incorrect device is contained in the package. The packaging label indicates that the device is for left side use, the product inside the package is for right side use. Use of an opposite side mesh can result in implant failure and hernia recurrence
Covidien is recalling a specific type of hernia repair mesh because it was shipped with the wrong side (right instead of left) for the repair. Using this incorrect mesh can cause the hernia to come back or fail.
The mesh was labeled for left-side use but contains right-side mesh. When used on the left side, the mesh may not fit properly, leading to hernia recurrence or implant failure.
People who received this specific mesh for inguinal hernia repair (left side) but used the right-side mesh are at risk. Surgeons and patients who had the procedure with this mesh are most affected.
Check for item code TECT1510AL and lot number SUH0709M on the packaging. The mesh is 15 cm x 10 cm polyester and designed for left-side hernia repairs.
Look for item code TECT1510AL and lot number SUH0709M on the packaging to confirm if it's the recalled product.
The mesh was shipped with the wrong side (right instead of left) for the repair, which can cause hernia recurrence or implant failure.
Check the item code and lot number on the packaging. If it matches TECT1510AL and SUH0709M, contact Covidien for guidance.
No, using the wrong side mesh can cause hernia recurrence or implant failure, so it should not be used for left-side repairs.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1142-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1142-2021 from Covidien. 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.
