FDA Medical Device Recalls (openFDA)
Whele LLC DBA Perch: Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Blue Electric Heating Pad, MB-001
- Recall number
- Z-0236-2023
- Recalling firm
- Whele LLC DBA Perch
- Product
- Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Blue Electric Heating Pad, MB-001
- 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
- 528,067
- Distribution
- US Nationwide through Amazon.com and Walmart.
- Lot, serial or model codes
- No UDI Lots: 210108 210305 210805 211002 210109 210306 210806 211003 210110 210307 210901 211004 210111 210308 210902 211005 210201 210309 210904 211006 210202 210310 210905 211007 210203 210405 210906 211008 210204 210406 210903 211009 210301 210407 210907 211010 210401 210501 210908 211101 210402 210502 210909 211102 210403 210801 210910 211103 210302 210802 210911 211104 210303 210803 210912 211105 210304 210804 211001 211106 211107 211108 211201 211202 211203 211204 211205 211206 211207 220101 220201 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