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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 4041–4060 of 4599 recalls

Ethicon Endo-Surgery Inc: ENDOPATHETS-Flex Endoscopic Linear Cutter, ATW35 Utilize...

The firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.

FDAApr 24, 2008PR• Ethicon Endo-Surgery Inc

Ethicon Endo-Surgery Inc: ENDOPATHETS and ETS-Flex Endoscopic Linear Cutter Reload;...

The firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.

FDAApr 24, 2008PR• Ethicon Endo-Surgery Inc

Ethicon Endo-Surgery Inc: FlexTray"Procedure Delivery System ENDOPATH; FBW67XL, FD0...

The firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.

FDAApr 24, 2008PR• Ethicon Endo-Surgery Inc

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GE Healthcare: GE Datex-Ohmeda Engstrom Carestation The Carestation cons...

There is a correction associated with Engstrom Carestation with an integrated Aerogen Professional Nebulizer System. There is an issue relating to the removal of the nebulizer cable from nebulizer connection port, which, when done while the nebulizer is active, may result in the discontinuance of mechanical ventilation. This issue affects all of the Engstrm Carestations shipped between 12/4/2006

FDAApr 23, 2008GA, IN, NM +5 more• GE Healthcare

Genzyme Corporation: Equal Diagnostics Lipase Color Reagent Kit Part Number: ...

Calibration and Quality Control outside of established range resulting from an increase in initial OD readings with the reagent contained within the kits.

FDAApr 14, 2008Nationwide• Genzyme Corporation

Genzyme Corporation: Seprafilm Adhesion Barrier (chemically modified sodium hy...

Sterility may be compromised

FDAApr 10, 2008Nationwide• Genzyme Corporation

GE Healthcare: GE Healthcare Solar 8000M System, a multiparameter physio...

A software error has been discovered when using Combination Monitoring with Solar 8000M/i - PDM - Telemetry in combo mode. This error has only been noted with this particular configuration and mode of monitoring. It has not been observed in other monitoring applications. The software error will result in a reset of the Solar 8000M/i, causing a loss of monitoring for approximately 1-2 minutes a

FDAApr 2, 2008Nationwide• GE Healthcare

Serenity Spa Hot Tubs (Gecko Alliance) – electrical fire hazard (2008)

Fire/Burn Risk

This recall involves the Hydropool Serenity Series Spa hot tubs with serial numbers 01350XXXX through 03210XXXX. The serial numbers are printed on the right side of the spa control. The Gecko spa control (SSPA-1) has model number 0202-205097 printed on it.

CPSCApr 1, 2008Nationwide• Gecko Alliance of Quebec, Canada

GE Healthcare: GE Voluson E8 Ultrasound System with software versions 6....

Inaccurate dimension measurements in M-Mode when pan-Zoom is activated in GE Voluson E8 Ultrasound Systems. Of particular concern are potential inaccuracies of fetal cardiac measurements that may impact patient safety.

FDAApr 1, 2008AL, AZ, AR +45 more• GE Healthcare

Smith And Nephew, Inc. Wound Management Division: FLAT DRAIN -10MM, CHARIKER-JETER DRESSING KITS (LARGE AND...

Incorrect labeling. Kit labels may incorrectly state that a flat drain is contained as a kit component while some kits may contain a round drain.

FDAMar 31, 2008Nationwide• Smith And Nephew, Inc. Wound Management Division

GE Healthcare: GE 1.5T and 3.0T Signa HDX MR System Model Number(s): 22...

Possible misdiagnosis or inappropriate treatment based on the image. Signal homogeneity may be affected when BRAVO applications are set with IR Prep off. The concern is that signal inhomogeneity can result in an erroneous diagnosis.

FDAMar 28, 2008AL, AK, AZ +43 more• GE Healthcare

Integra Pain Management: Integra LifeSciences Corporation Disposable Convenience K...

Hep-Lock Flush vials included in Integra's PICC Insertion Trays contain a heparin component that has been recalled by Baxter for contaminated heparin.

FDAMar 18, 2008CO• Integra Pain Management

GE Healthcare: DST-XL Model 1002375 is a multi-head, whole body gamma ca...

GE Healthcare has recently became aware of a cable failure associated with the arm or gantry rotation of the DST-XL Camera that may impact patient safety.

FDAMar 10, 2008AL, AR, CA +21 more• GE Healthcare

GE Healthcare: GE Healthcare Definium 8000 Digital Radiographic System.

Radiation dose reading greater than actual dose: Error in the generator software on the GE Healthcare Revolution XR/d configured with HP 8200 PC consoles and all Definium 8000 systems may impact patient safety. Occasional generator software errors may cause light X-ray Images with reported mAs readings higher than was actually exposed to the patient using the overhead X-ray tube. The mAs rea

FDAMar 7, 2008Nationwide• GE Healthcare

GE Healthcare: GE Healthcare Definium 8000 Digital Radiographic System. ...

Loss of image data: Software anomaly in the Processing Software on the Definium 8000 system may impact patient safety when using the VolumeRAD advanced application (option). The slice visualization of VolumeRAD exams acquired on the Wallstand receptor will be offset by 17mm. This prevents the visualization of anatomy WITHIN a distance of 17mm from the wallstand patient barrier (receptor cover).

FDAMar 7, 2008Nationwide• GE Healthcare

GE Medical Systems, LLC: GE Innova 3100 / 3100 IQ, Cardiovascular Imaging System, ...

GE Healthcare reported an issue with the Exposure Switch Redundancy system with Innova Systems 3100 & 4100, in which this error stays on, even after the pedal is released, inhibiting further x-rays, and a system reset is required to recover.

FDAMar 6, 2008MD, TX, VA• GE Medical Systems, LLC

GE Medical Systems, LLC: Innova 4100 / 4100 IQ, GE Healthcare, Waukesha, WI 53188 ...

FDAMar 6, 2008MD, TX, VA• GE Medical Systems, LLC

Medtronic Cardiac Surgery Technologies: VNUS Medical U-CLIP Removal Tool, UREM1860, is intended f...

Medtronic has identified one lot #0610315 of U-Clip Removal Tools, Catalog UREM1860FW, that was incorrectly assembled. The nose cone attachment, on the body of the removal tool, may not contain sufficient adhesive, which can allow the nose cone to separate from the body of the device.

FDAFeb 25, 2008AZ, CA, FL +10 more• Medtronic Cardiac Surgery Technologies

GE OEC Medical Systems, Inc: OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 98...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. The vertical lift column power supply in the mainframe C-arm of the device is defective and subject to early life failure.

FDAFeb 22, 2008Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 98...

Class IHigh

FDAFeb 22, 2008Nationwide• GE OEC Medical Systems, Inc