Ethicon recalls Ethibond Excel 36-inch sutures due to silicone curing issues during manufacturing. Affected products have specific model and lot numbers. Consumers should check details to determine if their item is recalled.
Identified curing issues with the silicone during the needles manufacturing process.
Ethicon is recalling Ethibond Excel 36-inch surgical sutures because of potential silicone curing problems during production. This could affect the suture's safety and performance during use. If you own this product, check the lot number and model to see if it's affected.
The silicone in the sutures may not cure properly during manufacturing, which could lead to weaker or inconsistent material. This might affect the suture's strength and reliability during medical procedures.
Surgical professionals and patients who use Ethibond Excel 36-inch sutures for procedures. Those with the specific lot numbers listed in the recall are most at risk.
Check the product label for the model number ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH and lot number 10489X. The product code X843H-56 and GMDN 13906 also help identify affected items.
Look for the model number ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH and lot number 10489X on the product label.
The recall states there are identified curing issues with the silicone, but the risk level is low. The product may not cure properly during manufacturing, which could affect strength.
Check the product label for the model number ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH and lot number 10489X. The product code X843H-56 and GMDN 13906 also help identify affected items.
The recall does not specify a remedy, so you should check the product details to see if it's affected. If it is, contact Ethicon for further instructions.
We’ve drafted a message you can send Ethicon to request your refund or repair — edit it as you like.
Subject: Recall Z-1516-2025 — Ethicon Ethicon Hello, I own a Ethicon that is covered by recall Z-1516-2025 from Ethicon. 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.
