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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

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 3941–3960 of 4599 recalls

ConMed Electrosurgery: ABC Bend-A-Beam Handpiece REF 134003 Handcontrol Malleabl...

The internal electrode protrudes in front of the ceramic insulator at the tip of the handpiece.

FDADec 18, 2008Nationwide• ConMed Electrosurgery

ConMed Electrosurgery: ABC PROBE REF 160644 5 mm Handswitching Probe, 44 cm QTY:...

The internal electrode can protrude in front of ceramic insulator at the tip of the ABC Handpiece used with Conmed Electrosurgical units.

FDADec 18, 2008Nationwide• ConMed Electrosurgery

GE Healthcare Integrated IT Solutions: Centricity Enterprise Web 3.0 software; the software allo...

Software error: There are two potential safety situations with Centricity Enterprise Web software - a forced log off may occur while using the Centricity Enterprise Web during an open session, and Centricity Enterprise Web does not utilize calibration performed on image measurements in Centricity RA1000 Workstation.

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FDADec 12, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

There is a potential patient safety issue involving the use of the F12 keyboard Approve & Complete function. The issue may cause erroneous information to be added to a report when trying to approve and complete it.

FDADec 12, 2008Nationwide• GE Healthcare Integrated IT Solutions

Commercial Frozen Food Merchandisers (Tyler) – Fire Hazard (2008)

Fire/Burn Risk

The recalled Vertical Multi-deck Frozen Food Merchandisers are typically used in grocery stores and other commercial settings. The recall involves models D6F, D6FL, L6F, L6FL, N6F and N6FL manufactured between 1995 and 2008. The serial and model numbers are located on the label located on the inside, upper-right front of the unit behind the lighting assembly. A complete list of the serial numbers involved in this recall can be found at www.tylerrefrigeration.com

CPSCDec 11, 2008Nationwide• Tyler Refrigeration, of Niles, Mich.

Ethicon Endo-Surgery Inc: Ethicon Endo-Surgery ENDOPATH Electrosurgery Probe Plus I...

Nickel exposure: The stainless steel tips on the affected product were degrading, causing a small amount of nickel to be released, which may lead to health risks in some patients, particularly those with a known or suspected nickel allergy or sensitivity. Ethicon Endo-Surgery determined the presence of free nickel in the affected product could elicit a reaction in those patients with nickel sens

FDADec 9, 2008PR• Ethicon Endo-Surgery Inc

Theragenics Corporation: Spacers of varying lengths used with the InSTANT Strandin...

Some pouches were found to have weak seals potentially compromising sterility.

FDADec 8, 2008Nationwide• Theragenics Corporation

GE Medical Systems, LLC: GE Healthcare CT/e and HiSpeed X/i, families of computed ...

During internal testing, GE Healthcare has recently determined that the collimator used on our CT/e and HiSpeed X/i families of Computed Tomography systems does not comply with the specific requirements in United States Title 21 of the Code of Federal Regulations, and IEC 60601-1-3, related to leakage radiation from the diagnostic source assembly, which includes the collimator. The excess leak

FDADec 1, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: Sytec 6000, Sytec 8000, and Lemage/ProSeed/ProSpeed famil...

FDADec 1, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: Innova 2121-IQ/3131-IQ Biplane Cardiovascular Imaging Sys...

GE Healthcare has become aware of a potential image storage failure on Innova 2121 IQ/ 3131 IQ cardiovascular imaging systems that may impact patient safety. This intermittent communication failure on the image storage chain may result in the following situations: Record abort, Record not available, Fluorostore function not available, Review not available, Boot/Reset failure. Fluoroscopy imag

FDANov 21, 2008CA, CO, FL +19 more• GE Medical Systems, LLC

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

There is a potential patient safety issue involving patient jacket content, which may result in unintended historical image(s) being displayed.

FDANov 21, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

Unread exams may inadvertently get marked as dictated in PACS workstation when the user signs off the report in Talkstation and opens the next exam.

FDANov 20, 2008CA, FL, IL +8 more• GE Healthcare Integrated IT Solutions

GE Wall Ovens – Fire and Burn Risk (2008)

Fire/Burn Risk

This recall involves GE wall ovens sold under the following brand names: GE®, GE Profile™, Monogram® and Kenmore®. The wall ovens were sold in white, black, bisque and stainless steel. The following model and serial numbers can be found inside the oven on the left interior wall. For microwave combination ovens, the serial number can be found on the left interior wall of the microwave. Brand Model Serial Number Begins With GE/Profile JCT915, JT912, JT915, JT952, JT955, JT965, JT980*, JTP20, JTP25, JTP28, JTP48, JTP50, JTP86 TD, VD, ZD AF, DF, FF, GF, HF, LF, MF, RF, SF, TF, VF, ZF Monogram ZET3058, ZET938, ZET958 Kenmore (All model numbers start with 911) 4771, 4775, 4781, 4904, 4905, 4923* 2T, 2V, 2Z 3A, 3D, 3F, 3G, 3H, 3L, 3M, 3R, 3S, 3T, 3V, 3Z * Lower oven only

CPSCNov 18, 2008Nationwide• GE Consumer & Industrial, of Louisville, Ky.

GE Healthcare Integrated IT Solutions: Centricity TriWin Laboratory Information System; GE Healt...

A software defect in the Centricity Lab (TriWin) product may incorrectly link patient information to a wrong report. Also, when viewing results in Patient Viewer, and a coagulation result is higher or lower than the linearity limit, then all of the results following the higher or lower result will show the same result as the first flagged result.

FDANov 17, 2008Nationwide• GE Healthcare Integrated IT Solutions

CORAL Swim 'N Score Pool Stix (ERO Industries) – Impalement Risk (2008)

The recalled Pool Stix are weighted plastic tubes, which stand upright when tossed into water. The sticks are about 8" long and were sold in packs of 6 in various colors. The UPC (#4969382814) is printed on the product's packaging.

CPSCNov 13, 2008Nationwide• ERO Industries (no longer in business), of Mount Prospect, Ill.

BD Diagnostics (GeneOhm Sciences, Inc): BD Diagnostics, BD GeneOhm MRSA Assay, REF: 441242 (200 R...

BD Diagnostics GeneOhm (BDDG) has determined that the Cepheid SmartCycler reaction tubes packaged in the BD GeneOhm MRSA test kits identified above may be defective.

FDANov 11, 2008CA, IL, IN +15 more• BD Diagnostics (GeneOhm Sciences, Inc)

GE Medical Systems, LLC: GE Innova 4100/4100 IQ. , GE Healthcare, Waukesha, WI 531...

One of three copper spectral filters could remain within the x-ray while the system displays no spectral filter. The displayed Air Kerma rate and thus cumulative Air Kerma are overestimated. The Air Kerma rate may be over estimated by up to 60%.

FDANov 4, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Healthcare Ventri, GE Healthcare, Waukesha, WI. Model ...

GE Healthcare become aware of an incident which caused a slight patient injury during his unload following a prone-oriented scan on Ventri. Although clear safety instructions were not followed in this case, additional measures will be implemented in an effort to reduce the probability or repeat occurrence.

FDANov 3, 2008AL, AZ, AR +35 more• GE Medical Systems, LLC

GE Medical Systems, LLC: Signa Openspeed 0.7T MR Systems, Model Numbers: Openspee...

GE Healthcare has identified a potential pinch point hazard on Ovation MR Scanner when using CTL Array XL Body Flex and Opened Body coil. A patient's hand may be pinched between the magnet bore ceiling cover and the CTL Array, XL Body Flex, or Open Body coil if the patient puts his/her hand on the top of the coil. Two injuries and four complaints filed. 2/20/09: Recall being expanded to incl

FDANov 3, 2008AL, AR, CA +36 more• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Healthcare Signa Ovation 0.35T, Model Numbers: Ovation...

GE Healthcare has identified a potential pinch point hazard on Ovation MR Scanner when using CTL Array XL Body Flex and Opened Body coil. A patient's hand may be pinched between the magnet bore ceiling cover and the CTL Array, XL Body Flex, or Open Body coil if the patient puts his/her hand on the top of the coil. 2/20/09: Recall being expanded to include the OpenSpeed Systems.

FDANov 3, 2008AL, AR, CA +36 more• GE Medical Systems, LLC