FDA Medical Device Recalls (openFDA)
Whele LLC DBA Perch: Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Grey Electric Heating Pad, PE-MtyBls-HeatPad-12x24-Gry-V2
- Recall number
- Z-0238-2023
- Recalling firm
- Whele LLC DBA Perch
- Product
- Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Grey Electric Heating Pad, PE-MtyBls-HeatPad-12x24-Gry-V2
- Status
- Open, Classified
- Initiated
- 2022-10-24
- Posted
- 2022-11-23
- Terminated
- not on file
- Reason
- The products may have the potential to burn customers. Firm has received complaints of burns, mild shocks, and rashes/irritation.
- Root cause
- Device Design
- Action
- On October 24, 2022, the firm notified retailers Amazon.com and Walmart of the recall. These internet retailers were instructed to notify users of the product about the recall using their customer information. Whele LLC will also have a website for the public that will include instructions for the recall as well as customer support for the recall. The website can be found at https://www.mightyblissheatingpadrecall.expertinquiry.com/ Users are asked to immediately cease use of the product and safely destroy the product by cutting the cord (after ensuring the product is unplugged.) Users are asked to take a photo of the destroyed product and upload it to the firm's recall website to verify that the product can no longer be used. Firm also issued press release: https://www.prnewswire.com/news-releases/whele-llc-announces-national-voluntary-recall-of-mighty-bliss-electric-heating-pad-due-to-product-safety-concerns-301656419.html
- Quantity
- 4,034
- Distribution
- US Nationwide through Amazon.com and Walmart.
- Lot, serial or model codes
- No UDI Lots: 220103
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IRT
- Firm FEI
- 3016774562
- Firm city
- Boston
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28