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Ethicon Endo-Surgery Inc

Ethicon Endo-Surgery Inc Recalls

All product recalls associated with Ethicon Endo-Surgery Inc.

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Recall Summary

Total Recalls

1000

Past Year

421

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 3341–3360 of 4599 recalls

Ethicon Endo-Surgery Inc: PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin...

Fire/Burn Risk

The device may have a non-conforming component that may cause the device to fire an unformed staple.

Class IIModerate

FDAAug 12, 2014Nationwide• Ethicon Endo-Surgery Inc

GE Healthcare, LLC: CARESCAPE Respiratory Modules E-sCO, E-sCOV, E-sCAiO, E-s...

GE Healthcare has recently become aware of a potential safety issue due to a failure of an O2 sensor component associated with the CARESCAPE respiratory modules, the Airway Gas Option and their respective service exchange units.

Class IIModerate

FDAAug 8, 2014CA, CO, FL +15 more• GE Healthcare, LLC

RegeneSlim Appetite Control (Regeneca) – DMAA Contamination (2014)

RegeneSlim was found to contain DMAA by FDA analysis.

1...166 167168169 170...230

Page 168 of 230Next

Class IIModerate

FDAAug 4, 2014Nationwide• Regeneca, Inc

Lightolier Glass Lens (Philips) – Laceration Hazard (2014)

Laceration Risk

This recall involves Philips "Lightolier" brand AF4SY decorative glass lenses used on various types of light fixtures. The clear glass lens, used to "soften" light with an additional lens layer, is 4 ¾ inches in diameter and 1/8 inch thick. The lenses were manufactured between January 2007 and December 2013. There are no markings on the product. The product number is on the packaging.

CPSCJul 29, 2014Nationwide• Gray Glass Company, of Queens Village, NY

Oxycodone Hydrochloride Oral Solution (Boehringer) – preservative failure (2014)

Failed Stability Specifications: Out of specification result for preservative sodium benzoate.

Class IIILow

FDAJul 28, 2014Nationwide• Boehringer Ingelheim Roxane Inc

Organic Chunks of Energy Carob Supergreens (Natural Grocers) – potential contamination (2014)

Salmonella

Natural Grocers by Vitamin Cottage is recalling Chunks of Energy Carob Greens and Chunks of Energy Date Flax/Tumeric due to the potential presence of Salmonella.

Class IHigh

FDAJul 25, 2014Nationwide• Natural Grocers by Vitamin Cottage

Organic Chunks of Energy Date Flax Turmeric (Natural Grocers) – potential contamination (2014)

Salmonella

Natural Grocers by Vitamin Cottage is recalling Chunks of Energy Carob Greens and Chunks of Energy Date Flax/Tumeric due to the potential presence of Salmonella.

Class IHigh

FDAJul 25, 2014Nationwide• Natural Grocers by Vitamin Cottage

GE Healthcare, LLC: GE Healthcare, Discovery XR656P/N 5374989/5397837 is inte...

GE Healthcare has become aware of a potential safety issue involving the nylon hooks which support the FlashPad" detector on the Discovery XR656 wall stand systems. There have been reported incidents of detector falls, but no injuries have been reported.

Class IIModerate

FDAJul 25, 2014AL, CA, CO +28 more• GE Healthcare, LLC

2009 VOLKSWAGEN TIGUAN Recall: FUEL SYSTEM, GASOLINE

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain model year 2009-2014 Tiguan vehicles manufactured July 2007 to June 2014. When using winterized fuel, in certain conditions bubbles may form in the fuel system which could result in the vehicle stalling.

NHTSAJul 21, 2014Nationwide• VOLKSWAGEN

BD Biosciences, Systems & Reagents: BD Multi Check CD4 Low Control Catalog No. 340916 is int...

The outer box label contains the incorrect distribution date: Box states 2017-09-02 ; should be 2014-09-02

Class IIILow

FDAJul 18, 2014CA, GA, IN +6 more• BD Biosciences, Systems & Reagents

Clonidine HCl Injection (X-Gen) – labeling error (2014)

Labeling: Label Error On Declared Strength: The side label description incorrectly states "Each mL contains 500 mcg Clonidine Hydrochloride" instead of stating "Each mL contains 100 mcg Clonidine Hydrochloride".

Class IIILow

FDAJul 17, 2014Nationwide• X-Gen Pharmaceuticals Inc.

Genesis BPS, LLC.: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx O...

Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.

Class IIModerate

FDAJul 17, 2014Nationwide• Genesis BPS, LLC.

Genesis BPS, LLC.: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syrin...

Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.

Class IIModerate

FDAJul 17, 2014Nationwide• Genesis BPS, LLC.

Genesis BPS, LLC.: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoj...

Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.

Class IIModerate

FDAJul 17, 2014Nationwide• Genesis BPS, LLC.

2015 VOLKSWAGEN GOLF Recall: STEERING

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain model year 2015 Golf and GTI vehicles manufactured January 27, 2014, to May 12, 2014. In the affected vehicles, the stabilizer link fasteners may come loose and possibly interfere with the steering of the vehicle.

NHTSAJul 7, 2014Nationwide• VOLKSWAGEN

2014 GENUINE SCOOTER STELLA Recall: ELECTRICAL SYSTEM:IGNITION:MODULE

Genuine Scooters, LLC (Genuine) is recalling certain model year 2014 Stella 125 Automatic scooters manufactured December 2013 to March 2014. The affected scooters may have a faulty engine control unit (ECU) which can cause the engine to stall without warning.

NHTSAJul 7, 2014Nationwide• GENUINE SCOOTER