The Recall Desk
Agency classClass IOur severity:SevereFDA (Devices)·Z-0237-2023·Announced 2022-11-30

Mighty Bliss Electric Heating Pad Recalled for Burn and Shock Risk

Whele LLC is recalling the Mighty Bliss Electric Heating Pad due to burn and shock hazards. The company has received complaints of burns, electrical shocks, and skin irritation.

The agency’s classification

FDA (Devices): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: This product carries an FDA Class I medical device classification, which requires a minimum score of 4. The firm has received documented complaints of actual burns, electrical shocks, and skin irritation, confirming that injury has been reported.

Plain-English summary

Whele LLC DBA Perch is recalling the Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 inches), model MB-002, in blue. Approximately 12,140 units were distributed nationwide through Amazon.com and Walmart. The product has the potential to burn customers.

The firm has received complaints of burns, mild electrical shocks, and rashes or skin irritation associated with the product. This is a Class I recall from the U.S. Food and Drug Administration.

Additional information about this recall is available from the FDA.

The recalled product

Product
Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 ) Blue Electric Heating Pad, MB-002
Manufacturer
Whele LLC DBA Perch
Category
Medical Device — Heating Appliance
Hazard
Affected units
12,140

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • No UDI Lots: 210901 211001

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 3 recalled by Whele LLC DBA Perch under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

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