Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CooperSurgical Wallach Loop Electrode 10mm x 10mm Square P/N: 909131. Recalled by CooperSurgical, Inc. Due to The affected Wallach LOOP Electrodes were incorrectly packaged...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact CooperSurgical, Inc. directly.
Affected Products
CooperSurgical Wallach Loop Electrode 10mm x 10mm Square P/N: 909131. Disposable Universal Electrodes, LOOP electrodes, used for electro-excisional procedures, and for electro-fulguration procedures of the lower genital tract
Quantity: 20 boxes of 5 each
Why Was This Recalled?
The affected Wallach LOOP Electrodes were incorrectly packaged with a Round Electrode inside a package labeled as a Square Electrode.
Where Was This Sold?
This product was distributed to 6 states: CA, MD, MO, NJ, PA, TX
About CooperSurgical, Inc.
CooperSurgical, Inc. has 83 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report