Vermed A10091-30Recalls & reported problems
Graphic Controls Acquisition Corp · ECG Monitoring Electrodes · Class 2
Quick summary
This Vermed ECG monitoring electrode has 119 adverse event reports, with 119 injuries and no deaths. Most describe skin irritation, itching and blisters, and some describe burning, redness and rash treated with prescription creams. Reports rose from 23 in the prior 12 months to 92 in the last 12 months. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 132
- Deaths reported
- 0
- Injuries reported
- 132
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 132 adverse event reports that list this exact device (DI 10009336008343), received between Nov 1, 2023 and Sep 24, 2026 — classified as 132 injuries.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem132
Patient problems
- Skin Inflammation/ Irritation118
- Itching Sensation52
- Blister50
- Erythema31
- Rash27
- Burning Sensation26
- Burn(s)3
- Peeling2
Recent adverse event reports
The 25 most recent of 132 reports, in the reporter's own words as published by the FDA.
InjurySep 24, 2026Adverse Event Without Identified Device or Use Problem
Patient reported skin irritation in the form of rash and hives. The patient sought medical treatment and was treated with a prescription oral antihistamine. The patient reported following proper skin preparation steps.
Patient problems: Rash; Skin Inflammation/ Irritation
MAUDE report 50881822 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
The patient reported experiencing skin irritation in the form of general redness, irritation, and itching. Medical treatment was sought and the patient was treated with a prescription topical anti-inflammatory medication. The patient reported following the recommended skin preparation steps.
Patient problems: Erythema; Skin Inflammation/ Irritation
MAUDE report 50794845 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
The patient reported experiencing skin irritation in the form of a rash and open sores, describing the skin as looking "burnt" and becoming raw and aggravated. Medical treatment was sought and the patient was prescribed both oral and topical steroids. The patient reported following the recommended skin preparation steps.
Patient problems: Rash; Skin Inflammation/ Irritation
MAUDE report 50794733 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
The patient reported experiencing skin irritation in the form of a rash, bleeding/discharge, and rawness with open skin. Medical treatment was sought and the patient was prescribed both oral and topical steroids. The patient reported following the recommended skin preparation steps.
Patient problems: Rash; Skin Inflammation/ Irritation
MAUDE report 50794589 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
The patient reported experiencing skin irritation in the form of general redness, raised skin, blisters/welts, and scabbing. Medical treatment was sought and the patient was treated with a prescription topical steroid. The patient reported following the recommended skin preparation steps.
Patient problems: Blister; Erythema; Skin Inflammation/ Irritation
MAUDE report 50794149 ↗InjurySep 11, 2026Adverse Event Without Identified Device or Use Problem
The patient reported a burning sensation and hives. The patient sought medical treatment and was prescribed a topical anti-inflammatory medication. The patient confirmed following the proper skin preparation steps.
Patient problems: Burning Sensation
MAUDE report 50732942 ↗InjurySep 11, 2026Adverse Event Without Identified Device or Use Problem
The patient reported skin irritation in the form of an allergic reaction of unknown type. The patient sought medical treatment and was prescribed medication. The patient did not follow proper skin preparation steps.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 50732936 ↗InjurySep 11, 2026Adverse Event Without Identified Device or Use Problem
Patient reported skin irritation in the form of hives. The patient sought medical treatment and was prescribed triamcinolone, an oral steroid. The patient reported following the proper skin preparation steps.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 50732933 ↗InjurySep 11, 2026Adverse Event Without Identified Device or Use Problem
The patient reported skin irritation in the form of itching and open sores. The patient sought medical treatment and was treated with prescription medication (topical steroid). The patient reported following the proper skin preparation steps.
Patient problems: Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 50732929 ↗InjurySep 4, 2026Adverse Event Without Identified Device or Use Problem
Patient reported skin irritation in the form of general redness, irritation, and red bumps with no open skin. The patient sought medical treatment and was treated with a prescription topical anti-inflammatory medication. The patient followed the recommended skin preparation steps.
Patient problems: Erythema; Skin Inflammation/ Irritation
MAUDE report 50619223 ↗InjurySep 4, 2026Adverse Event Without Identified Device or Use Problem
The patient reported experiencing a rash. Medical treatment was sought and the patient was treated with a prescription topical steroid. The patient reported following the recommended skin preparation steps.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 50618549 ↗InjurySep 4, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Erythema; Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 50618168 ↗InjuryAug 26, 2026Adverse Event Without Identified Device or Use Problem
The patient reported skin irritation in the form of itching. Patient sought medical treatment and was perscribed Mometasone Furoate 0.01%, a topical anti-inflammatory medication. The patient followed the recommended skin preparation steps.
Patient problems: Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 50452734 ↗InjuryAug 25, 2026Adverse Event Without Identified Device or Use Problem
The patient reported experiencing burning sensations, general redness, itching, and blisters/welts. Medical treatment was sought and the patient was treated with a prescription topical anti-inflammatory medication. The patient reported following the recommended skin preparation steps.
Patient problems: Blister; Erythema; Skin Burning Sensation; Skin Inflammation/ Irritation
MAUDE report 50439809 ↗InjuryAug 20, 2026Adverse Event Without Identified Device or Use Problem
The patient reported skin irritation in the form of hives. The patient sought medical attention and was prescribed a medication. The patient followed the proper skin preparation guidelines.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 50344024 ↗InjuryAug 5, 2026Adverse Event Without Identified Device or Use Problem
Patient reported skin irritation in the form of itching, rash, and blisters/welts. The patient sought medical treatment and was treated with prescription medication. The patient did not follow proper skin preparation steps.
Patient problems: Blister; Itching Sensation; Rash; Skin Inflammation/ Irritation
MAUDE report 50141001 ↗InjuryJul 31, 2026Adverse Event Without Identified Device or Use Problem
Patient reported skin irritation in the form of red, itchy skin. The patient sought medical attention and was prescribed Triamcinolone acetonide 0.1%. The patient did not follow proper skin preparation steps.
Patient problems: Erythema; Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 50097731 ↗InjuryJul 31, 2026Adverse Event Without Identified Device or Use Problem
Patient reported general redness and itching. The patient sought medical treatment and was prescribed Triamcinolone, a topical anti-inflammatory cream. Patient reported following the proper skin preparation steps.
Patient problems: Erythema; Itching Sensation
MAUDE report 50097730 ↗InjuryJul 22, 2026Adverse Event Without Identified Device or Use Problem
THE PATIENT REPORTED EXPERIENCING AN ALLERGIC REACTION, BLEEDING/DISCHARGE, AND OPEN SORES. MEDICAL TREATMENT WAS SOUGHT AND THE PATIENT WAS TREATED WITH A PRESCRIPTION TOPICAL ANTI-INFLAMMATORY MEDICATION. THE PATIENT REPORTED FOLLOWING THE RECOMMENDED SKIN PREPARATION STEPS.
Patient problems: Hypersensitivity/Allergic reaction; Skin Inflammation/ Irritation
MAUDE report 25906101 ↗InjuryJul 17, 2026Adverse Event Without Identified Device or Use Problem
THE PATIENT REPORTED SKIN IRRITATION IN THE FORM OF BURNING SENSATION, ITCHING, AND RAWNESS WITH NO OPEN SKIN. THE PATIENT SOUGHT MEDICAL TREATMENT AND WAS PRESCRIBED A TOPICAL STEROID. PATIENT RECOMMENDED FOLLOWING PROPER SKIN PREPARATION STEPS.
Patient problems: Burning Sensation; Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 25856418 ↗InjuryJul 2, 2026Adverse Event Without Identified Device or Use Problem
PATIENT REPORTED SKIN IRRITATION IN THE FORM OF ITCHING AND BLISTERS/WELTS. THE PATIENT SOUGHT MEDICAL TREATMENT AND WAS PRESCRIBED A TOPICAL STEROID MEDICATION. PATIENT REPORTED FOLLOWING THE PROPER SKIN PREPARATION STEPS.
Patient problems: Blister; Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 25693478 ↗InjuryJul 2, 2026Adverse Event Without Identified Device or Use Problem
PATIENT REPORTED BLISTERS/WELTS. THE PATIENT SOUGHT MEDICAL TREATMENT AND WAS PRESCRIBED MEDICATION. THE PATIENT DID NOT FOLLOW PROPER SKIN PREPARATION INSTRUCTIONS.
Patient problems: Blister
MAUDE report 25693471 ↗InjuryJun 25, 2026Adverse Event Without Identified Device or Use Problem
PATIENT REPORTED SKIN IRRITATION IN THE FORM OF BURNING SENSATION, ITCHING, RASH, OPEN SORES, AND RAWNESS. THE PATIENT SOUGHT MEDICAL TREATMENT AND WAS TREATED WITH A PRESCRIPTION MEDICATION. THE PATIENT REPORTED FOLLOWING PROPER SKIN PREPARATION.
Patient problems: Burning Sensation; Itching Sensation; Rash; Skin Inflammation/ Irritation
MAUDE report 25623034 ↗InjuryJun 25, 2026Adverse Event Without Identified Device or Use Problem
PATIENT REPORTED SKIN IRRITATION IN THE FORM OF BLISTERS, REDNESS, ITCHING, AND BURNING SENSATION. PATIENT SOUGHT MEDICAL TREATMENT AND WAS TREATED WITH A PRESCRIPTION TOPICAL STEROID MEDICATION. THE PATIENT REPORTED FOLLOWING PROPER SKIN PREPARATION.
Patient problems: Blister; Burning Sensation; Erythema; Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 25623021 ↗InjuryJun 17, 2026Adverse Event Without Identified Device or Use Problem
PATIENT REPORTED SKIN IRRITATION IN THE FORM OF A BURNING (SENSATION), GENERAL REDNESS, ITCHING, RAISED SKIN, AND RED BUMPS. THE PATIENT REACHED OUT TO THE ORDERING PCP AND WAS PRESCRIBED A STEROID LOTION. THE PATIENT REPORTED FOLLOWING PROPER SKIN PREPARATION STEPS.
Patient problems: Burning Sensation; Erythema; Itching Sensation; Skin Inflammation/ Irritation
MAUDE report 25532209 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.