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ConMed Corporation

ConMed Corporation Recalls

All product recalls associated with ConMed Corporation.

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Recall Summary

Total Recalls

1000

Past Year

888

Class I (Serious)

124

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 12361–12380 of 17593 recalls

CONMED PEDIATRIC R2 Multifunction Electrodes (ConMed) – Connection Design Issue (2014)

Philips Healthcare made changes to the design of the connection between multifunction electrodes and their HeartStart FR3 and HeartStart FRx AEDs. The failure to connect may result in a delay of therapy, which could result in patient death or serious injury.

Class IHigh

FDANov 6, 2014Nationwide• ConMed Corporation

CONMED ADULT R2 Multifunction Electrodes (ConMed) – Connection Design Issue (2014)

Class IHigh

FDANov 6, 2014Nationwide• ConMed Corporation

ADULT Radiotransparent Electrode (ConMed) – Connection Design Issue (2014)

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Class IHigh

FDANov 6, 2014Nationwide• ConMed Corporation

Healon EndoCoat Ophthalmic Device (Abbott) – Finger Grip Dislodgement (2014)

AMO has received complaints where the finger grip dislodged while depressing the syringe plunger. The finger grip dislodgement could result in the surgeon's hand unintentionally moving the cannula further than intended, resulting in potential trauma to the eye.

Class IIModerate

FDANov 6, 2014Nationwide• Abbott Medical Optics Inc (AMO)

MINI PEDIATRIC Radiotransparent Electrode (ConMed) – Connection Design Issue (2014)

Class IHigh

FDANov 6, 2014Nationwide• ConMed Corporation

PEDIATRIC Radiotransparent Electrode (ConMed) – Connection Design Issue (2014)

Class IHigh

FDANov 6, 2014Nationwide• ConMed Corporation

Cardiac Function Analysis Software (Toshiba) – Analysis Result Error (2014)

Potential problem with the cardiac function analysis software (CFA). Incorrect analysis results may be displayed in the Function Parameters for the Entire Heart displayed as analysis results of the CFA and in a Left-Ventricular Volume Curve generated based on some of those parameters.

Class IIModerate

FDANov 5, 2014Nationwide• Toshiba American Medical Systems Inc

Coca Cola Zero (Coca-Cola) – ingredient inconsistency (2014)

Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.

Class IIILow

FDANov 5, 2014IN, KY, OH• Coca-Cola Company (The)

Safety PICC Insertion Tray (Custom Healthcare) – Incorrect Item Number (2014)

An INCORRECT item number is packed within the OUTSIDE "PIGGYBACKED" PACKAGE. The interior sealed STERILE KIT is correct and NO adverse issues affect that part of the item. The NON-STERILE OUTSIDE "PIGGYBACKED" PACKAGE mistakenly contains ITEM #8881579121 - Syringe prefilled, Saline Flush, 09% Sodium Chloride and is a NONSTERILE PRODUCT that CANNOT BE DROPPED INTO THE STERILE FIELD.

Class IIModerate

FDANov 5, 2014CT• Custom Healthcare Systems, Inc.

Cardiac Function Analysis Software (Toshiba) – Analysis Result Error (2014)

Class IIModerate

FDANov 5, 2014Nationwide• Toshiba American Medical Systems Inc

MiniMed Infusion Sets (Medtronic) – Tubing Detachment Risk (2014)

Tubing may detach at the connect/disconnect location on the MiniMed Silhouette and MiniMed Sure-T infusion sets. Detachment causes interrupted insulin delivery and the pump will not alarm to notify your patient. This can lead to hyperglycemia, and diabetic ketoacidosis (DKA).

Class IIModerate

FDANov 4, 2014Nationwide• Medtronic MiniMed Inc.

Stellaris PC (Bausch & Lomb) – Software Transition Issue (2014)

Fire/Burn Risk

A software anomaly was identified where the system may automatically transition from "Standby" to "Ready to Fire" state while in surgical use.

Class IIModerate

FDANov 4, 2014AL, CA, CT +18 more• Bausch & Lomb Inc

McGrath MAC2 Video Laryngoscope Blades (Aircraft Medical) – Blade Connection Risk (2014)

The blade retaining clip may be difficult to engage and thereby increase the possibility of a blade becoming disconnected during intubation, specifically when the device is being retracted from the patients mouth.

Class IIModerate

FDANov 4, 2014Nationwide• Aircraft Medical Limited

BrightView Imaging System (Philips) – Software Concerns (2014)

Software issues

Class IIModerate

FDANov 4, 2014AR, CA, FL +14 more• Philips Medical Systems (Cleveland) Inc

Stellaris PC (Bausch & Lomb) – Software Transition Issue (2014)

Fire/Burn Risk

A software anomaly was identified where the system may automatically transition from "Standby" to "Ready to Fire" state while in surgical use.

Class IIModerate

FDANov 4, 2014AL, CA, CT +18 more• Bausch & Lomb Inc

Stellaris PC (Bausch & Lomb) – Software Transition Issue (2014)

Fire/Burn Risk

A software anomaly was identified where the system may automatically transition from "Standby" to "Ready to Fire" state while in surgical use.

Class IIModerate

FDANov 4, 2014AL, CA, CT +18 more• Bausch & Lomb Inc

GuardIVa IV Dressing (Bard) – Non-Sterile Sample Concern (2014)

Bard Access Systems is recalling GuardIVa (Ref. No. FP23AD006) from lot ASXHT003 because they were non-sterile unit samples which potentially could be used clinically.

Class IIModerate

FDANov 3, 2014AR, LA, OK +1 more• Bard Access Systems