Ethicon, LLC recalls ETHILON Nylon Suture, Product Code 697G
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,…
Read the official notice →- Date
- 2026-11-04
- Country
- United States
- Brand
- Ethicon
- Product
- ETHILON Nylon Suture, Product Code 697G
- Classification
- Class II
- Units
- International distribution to the countries of JP, CA, AU.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Ethicon recalls
- 2026-10-21
Ethicon, LLC recalls PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18" TF-5, Product Code: N271H
Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that if discovered prior to use may cause surgical delay. If…
FDA · DeviceEthicon, LLCWorldwide - US Nationwide distribution in the states of SC, PA, TX, CA, ID,…Official notice →- 2025-10-01
ETHICON, LLC recalls STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device, SFX SPI PDS+ BI VIO 14X14IN(36X36CM) USP1(M4) D/A MO-4. Product…
Potential for barb non-engagement.
FDA · DeviceETHICON, LLCWorldwide - US Nationwide distribution in the states of AR, AZ, CA, IL, IN,…Official notice →- 2025-02-12
Ethicon, LLC recalls PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general soft tissue…
Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to the patient and…
FDA · DeviceEthicon, LLCWorldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →- 2024-11-27
ETHICON, INC. recalls MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue approximation and/or…
Due a component mix-up in manufacturing, the affected products may contain incorrect needle type/size and suture length.
FDA · DeviceETHICON, INC.U.S.: AK, AL, AR, AZ, CA, CO,CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA,…Official notice →- 2024-11-13
Ethicon, Inc. recalls Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product Number J358H
Complaints were received regarding needle pull-off and suture degradation. Analysis on returned product from this lot confirmed that some sutures were visually degraded in the package.
- 2024-06-26
Ethicon, Inc. recalls PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric…
Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection .
FDA · DeviceEthicon, Inc.Worldwide distribution - US Nationwide including PR and the countries of AR,…Official notice →
Other drugs & medical recalls in the United States
- 2026-11-04
Philips North America recalls Model Number: 712010.
Potential for the device to fail immediately after an exposure, causing the system to remain stationary.
FDA · DevicePhilips North AmericaWorldwide Distribution: (US Nationwide) and International distribution to…Official notice →ZIEHM-ORTHOSCAN INC recalls Orthoscan VERSA Accessory Cart, REF: 1000-0021 and Versa Mini C-Arm System, REF: 1000-0020
The accessory cart weldment does not conform to weld dimensional specifications which may result in separation of the monitor arm mounting structure from the cart.
FDA · DeviceZIEHM-ORTHOSCAN INCWorldwide - US Nationwide distribution in the states of AZ , CA , CO , CT , FL…Official notice →Medtronic, Inc. recalls OmniaSecure Model 3930M, LEAD 3930M74 74 CM DF4 MR 3930M74 LEAD 3930M79 79 CM DF4 MR 3930M79 The Medtronic OmniaSecure" Model 3930M lead…
Affected leads require additional engineering evaluation due to complaints regarding difficulty in achieving fixation during implantation. Potential harm of tissue trauma due to implant difficulty.
FDA · DeviceMedtronic, Inc.US Nationwide distribution including in the states of AZ, CA, CT, DE, FL, GA,…Official notice →Abiomed, Inc. recalls Automated Impella Controller, Packaged. Primary user control interface for the Impella Catheter, catheter-based heart pump.
Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that may result in failure of the AIC to recognize the purge…
FDA · DeviceAbiomed, Inc.Worldwide Distribution: US (nationwide) and OUS (foreign) to countries:…Official notice →MSN Laboratories Private Limited (Formulations Division,… recalls Atorvastatin Calcium Tablets, USP, 40mg, 1000 tablets per bottle, Rx only, Manufactured by: MSL…
Presence of Foreign Tablets/Capsules
FDA · DrugMSN Laboratories Private Limited (Formulations Division,…Nationwide in the USA.Official notice →Brandywine Pharmaceuticals, LLC recalls Theophylline Extended-Release Tablets, 100 mg, Rx Only, 100-count bottle, Distributed by: Brandywine Pharmaceuticals, LLC, West…
CGMP Deviations: interruption in the ongoing stability testing program conducted at a third-party laboratory