3M recalls radiolucent ECG electrodes with foam tape due to potential carbon stud breakage. Affected units include specific lots and expiration dates. Consumers should check product details to determine if recalled.
Potential for breakage of the ECG electrode carbon stud from the eyelet.
3M is recalling radiolucent ECG electrodes with foam tape that may break, causing injury. This recall affects healthcare professionals using the electrodes for monitoring. The breakage could lead to skin irritation or other issues if the electrode fragments during use.
The carbon stud in the electrode can break from the eyelet, potentially causing skin irritation or injury if fragments are left on the skin. This breakage is a minor hazard that does not typically cause serious injury.
Healthcare professionals who use the 3M Red Dot Electrodes for ECG monitoring are most at risk. The recall applies to specific lots and expiration dates of the electrodes.
Check for the product name '3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape' and catalog number 2244. Affected units have specific lot numbers (202302LK to 202302LN) and expiration dates between February 19 and February 23, 2023.
Identify the product by checking the catalog number (2244) and lot numbers (202302LK to 202302LN) on the packaging.
The electrodes are safe for normal use but may break, causing minor skin irritation. 3M recommends checking if you have the recalled lot numbers.
Look for the catalog number 2244 and lot numbers 202302LK to 202302LN on the packaging. Expiration dates range from February 19 to February 23, 2023.
Check the product details to confirm if you have a recalled unit. If so, contact 3M for further instructions.
We’ve drafted a message you can send 3M to request your refund or repair — edit it as you like.
Subject: Recall Z-0188-2022 — 3M 3M Hello, I own a 3M that is covered by recall Z-0188-2022 from 3M. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
