Covidien recalls Force TriVerse electros: Risk of sterile packaging compromise. Affected units have specific item codes. Consumers should contact for remedy.
Potential for the sterile packaging to be compromised
Covidien is recalling its Force TriVerse electrosurgical device 10 due to potential compromise of sterile packaging. This could lead to infection risks during medical procedures if the device is used without proper sterility.
The sterile packaging might become damaged during shipping or handling, potentially exposing the device to contaminants. If the device is used without proper sterility, it could cause infections during surgery.
Healthcare professionals using the device in surgical settings. Patients undergoing procedures with this device are at risk if the packaging is compromised.
Check for item code FT3000F and lot number 80390309X on the packaging. The device is used in surgical procedures for cutting and coagulating tissue.
Reach out to Covidien for specific instructions on handling the recalled device.
The recall indicates potential packaging compromise, so it should not be used until the manufacturer provides instructions.
Contact Covidien directly for guidance on the next steps.
Look for item code FT3000F and lot number 80390309X on the packaging.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1020-2019 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1020-2019 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.
