FDA recall record

Coapt ControlSeal Electrode, cutaneous EMG Electrode recall — FDA Z-0204-2024

Patient may experience minor burn or blistering if device is exposed to direct sunlight and/or warm temperatures for over 12 hours or battery is damaged.

Class IIclassification
Z-0204-2024official record ID
Nov 8, 2023report date

Recall record at a glance

Official recordZ-0204-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCoapt LLC
Report dateNov 8, 2023
Recall initiation dateOct 2, 2023
Quantity109 devices
LocationChicago, IL, United States

Official product description

Coapt ControlSeal Electrode, cutaneous EMG Electrode

Why the product was recalled

Patient may experience minor burn or blistering if device is exposed to direct sunlight and/or warm temperatures for over 12 hours or battery is damaged.

Distribution information

Worldwide distribution - US Nationwide and the countries of Australia, Canada, and Sweden.

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: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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