FDA recall record

3M Company - Health Care Business 3M Red Dot Electrodes, Radiolucent Monitoring Electrode recall — FDA Z-0188-2022

Potential for breakage of the ECG electrode carbon stud from the eyelet.

Class IIclassification
Z-0188-2022official record ID
Nov 10, 2021report date

Recall record at a glance

Official recordZ-0188-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firm3M Company - Health Care Business
Report dateNov 10, 2021
Recall initiation dateOct 6, 2021
Quantity2,081,000 electrodes
LocationSaint Paul, MN, United States

Official product description

3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape, Catalog No. 2244, (3M ID (SKU): 70-2011-8506-6, SAP ID: 7100212989), packaged 10 electrodes per card, 5 cards per pouch, 20 pouches per shipper box, 1,000 electrodes total per shipper box. The 3M Red Dot Radiolucent Monitoring Electrode with Foam Tape 2244 is intended to be used by healthcare professionals for ECG monitoring. This electrode is disposable, intended for single use, and has been tested for up to 3 days wear.

Why the product was recalled

Potential for breakage of the ECG electrode carbon stud from the eyelet.

Distribution information

US Nationwide Distribution to states of: AL, AZ, CA, IA, IL, LA, MD, MO, NC, NJ, and OH; and OUS Foreign distribution to countries of: Australia, Bermuda, Canada, China, France, Germany, Japan, the Netherlands, Singapore, Sweden, and Turkey.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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