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Conmed Electrosurgery

Conmed Electrosurgery Recalls

All product recalls associated with Conmed Electrosurgery.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16221–16240 of 17592 recalls

Conmed Electrosurgery: Conmed System 2500 Electrosurgical Unit, REF 60-8011-SYS,...

Wrong size capacitor installed in electrosurgical generator could malfunction, causing muscle stimulation or delay in therapy.

FDASep 5, 2006Nationwide• Conmed Electrosurgery

Varian Medical Systems Inc: Clinac High Energy Medical Linear Accelerator, Medical Ch...

The chain holding the device gantry in position may break.

FDAAug 31, 2006Nationwide• Varian Medical Systems Inc

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 external defibrillator/monitor

Devices with v38 system software do not display a ''LOW BATTERY: CONNECT TO AC POWER'' message when the monitor is on backup (DC) battery power and may shut down without warning.

FDA

1...810 811812813 814...880

Page 812 of 880Next

Aug 30, 2006

Nationwide

• Medtronic Emergency Response Systems, Inc.

Garden Treasures Fireplace (Agio) – fire hazard (2006)

Fire/Burn Risk

The recalled fireplace consists of a round fire bowl that rests on four legs, with a chimney cap and hood. The fireplace is made of steel and is painted black. They are about 3 feet tall and 2 feet wide. The item number, 91023, is printed on the package materials.

CPSCAug 29, 2006Nationwide• Agio International Company, Limited, of Hong Kong

Beckman Coulter Inc: CXP Analysis Software, Versions 2.0 & 2.1: Part #722396 C...

Two workflow scenarios associated with renaming regions may produce incorrect results.

FDAAug 29, 2006Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Cytomics FC 500 MPL with MXP software, Versions 2.0 & 2.1...

Two workflow scenarios associated with renaming regions may produce incorrect results.

FDAAug 29, 2006Nationwide• Beckman Coulter Inc

Milano Counter Stools (FDL) – fall hazard (2006)

The recalled stools have four legs, are made of wood, and have dark brown or black seats. The counter stool is 24 inches tall and the bar stool is 30 inches tall. The stools have item numbers 202448 and 118136, which can be found on the packaging material.

CPSCAug 29, 2006Nationwide• FDL Inc., of Kokomo, Ind.

Beckman Coulter Inc: Cytomics FC 500 with CXP software, Versions 2.0 & 2.1: Pa...

Two workflow scenarios associated with renaming regions may produce incorrect results.

FDAAug 29, 2006Nationwide• Beckman Coulter Inc

X300 Lawn Tractors (John Deere) – blade operation risk (2006)

These John Deere X300 Select Series lawn tractors are green with yellow seats and wheels. The following model and serial numbers can be found on the serial number plate on the tractor's frame, which is located just above the front wheel axle on the right side of the tractor. Model Serial Number Ranges X300 M0X300A012380 - 012875 X300 M0X300C020339 - 024949 X300 M0X300D011842 - 012375 X304 M0X304A013047 - 013964 X320 M0X320A017344 - 020858 X324 M0X324A012658 - 013220 X340 M0X340A012667 - 013498

CPSCAug 29, 2006Nationwide• Deere & Company of Moline, Ill.

Nicolet Biomedical Div of Viasys Healthcare: NicoletOne version 5.20 software (also known as NicoletOn...

A software anomaly exists in the 5.20.1038 NicoletOne LTM, Sleep, nEEG, vEEG and ICU Monitor systems using the M, and/or C series amplifiers. If this anomaly occurs, the system will display the data for channel one in all channels on NicoletOne LTM, Sleep, nEEG, vEEG or ICU Monitor systems.

FDAAug 25, 2006Nationwide• Nicolet Biomedical Div of Viasys Healthcare

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10/10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Lawnmower Blades (Blount) – replacement defect (2006)

Laceration Risk

The recalled replacement lawnmower blades are intended for use on Snapper riding lawnmowers. The recalled blades are sold for use as replacement parts under the Oregon® and Silver Streak® brands only. Original equipment blades on Snapper lawnmowers and "Snapper" brand replacement blades are not included in this recall. The recalled blades are red and marked "MADE IN USA," "GRASS SIDE CX", "Oregon" or "SILVER STREAK." The part number and date code are engraved on one side of the blade. The recalled blades are part numbers: 99-111, 99-112, 99-113, 99-114, 99-117, 99-118, 99-926, 99-930 and date codes: BL, BM, BN, BP, BQ, BR, BS, BT, BU, BV, BW, BX, BY, BZ, CA, CB, CC, CD, CE, CF, CG, CH, CJ, CK, CL, CM, CN, CP.

CPSCAug 23, 2006Nationwide• Blount International Inc., of Kansas City, Mo.

Olympic Weightlifting Bars (York Barbell) – breaking units (2006)

This recall involves all 7' Int'l Hard Chrome 1000 lb. and 1500 lb. test Olympic bars with model number 32012 and 32013, 7' Int'l Black Oxide 1000 lb. and 1500 lb. test Olympic bars with model number 32020 and 32021, 7' International Men's Olympic Needle-bearing bars with model number 32010 and 6½' International Women's Olympic Needle-bearing bars with model number 32011. The bars have split sleeves and YORK is printed on the sleeve assemblies of each bar.

CPSCAug 23, 2006Nationwide• York Barbell Company Inc., of York, Pa.

EMD Chemicals Inc: Anaerotest;Microbiology , 50 test strips 1.15112 Store dr...

Lot # OC553145 of Anaerotest failed to remain in specification. QC indicator shows an anaerobic environment even if oxygen is present

FDAAug 17, 2006Nationwide• EMD Chemicals Inc

EMD Chemicals Inc: Anaerotest for microbiology Specification: Performance Te...

Lot # OC553145 of Anaerotest failed to remain in specification. QC indicator shows an anaerobic environment even if oxygen is present.

FDAAug 17, 2006Nationwide• EMD Chemicals Inc

GE OEC Medical Systems, Inc: GE OEC 9800 Fluoro C-Arm X-ray System, GE OEC Medical Sys...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

Cordless Electric Lawnmowers (Black & Decker) – fire hazard (2006)

Fire/Burn Risk

The mowers were sold under both the Black & Decker and Craftsman brand names. The recalled Black & Decker mowers have the model CMM1000 or CMM1000R and are labeled as Type 1 through Type 4, both of which are located on the silver and black label affixed to the rear door of the mower. Mowers labeled as Type 5 are not included in this recall. The Black & Decker mowers have either an orange or green deck with a black motor cover. The Craftsman brand mowers have model number 900.370520 and include all date codes and types. The model number is located on the silver and black label affixed to the rear door of the mower. The Craftsman mowers have a dark green deck with a black motor cover.

CPSCAug 16, 2006Nationwide• Black & Decker (U.S.) Inc., of Towson, Md.

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Digital Mobile C-Arm X-ray system, GE O...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: RUS Tool Version Software

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc