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Home › FDA recalls › ETHILON Nylon Suture
CLASS II · ModerateFDA

Ethicon, LLC recalls ETHILON Nylon Suture

📅 Sep 23, 2026 · 📍 CA
Recalling company
Ethicon, LLC
Product
ETHILON Nylon Suture, Product Code 697G
Reason
Nylon suture indicated for use in general soft tissue approximation and/or ligation may have needles with distorted curvature, that may break during use, or could cause additional soft tissue or vessel injury, including tearing or bleeding intraoperatively.
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Sep 23, 2026
Reported
Nov 4, 2026
Distribution
International distribution to the countries of JP, CA, AU.
Status
Ongoing
Quantity
4,003
Lot / codes
GTIN Box/Unit: 30705031008568/10705031008564. Lot: 10B3QS
Company location
San Lorenzo, PR
Recall type
Voluntary: Firm initiated
Recall number
Z-0284-2027
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0284-2027 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.