Covidien recalls specific Polysorb suture lots due to potential packaging issues that could affect humidity or sterility. Affected items may not be safe for surgery.
There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
Covidien is recalling certain Polysorb braided absorbable sutures because packaging might not keep them sterile or dry enough for surgery. This could lead to infections or other complications if used improperly.
The packaging might allow moisture or contaminants to enter, which could compromise the suture's sterility. This could lead to infections or other complications during surgery if the suture is not properly sterile.
Surgical professionals and hospitals using the specific suture lot D7H1092X with expiration date 2022-08-31 are most at risk. Patients receiving these sutures during surgery could face infection risks.
Check for the lot number D7H1092X on the packaging. The suture is 6-0 size, 18 inches, UNDYED SS-24 D/A, and expires by August 31, 2022.
Look for the lot number D7H1092X on the packaging to identify affected items.
The recall indicates potential packaging issues that could affect sterility or humidity, so it may not be safe for surgery. Affected lots should be checked and handled carefully.
If you have the specific lot D7H1092X, contact Covidien for guidance on next steps. The recall does not specify a return or disposal action.
Check for the lot number D7H1092X on the packaging. The suture is 6-0 size, 18 inches, UNDYED SS-24 D/A, and expires by August 31, 2022.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1292-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1292-2020 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.
