Stop using nowMedical device recall · FDA · Published October 24, 2022
Perch Mighty Bliss Electric Heating Pad Recall: Burn Risk
Perch recalls Mighty Bliss Extra-Large Blue Electric Heating Pads (MB-002) due to burn risk from mild shocks and rashes. Affected units sold with UDI lots 210901-211001.
“Perch Mighty Bliss Electric Heating Pad Recall: Burn Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59810-perch-mighty-bliss-electric-heating-pad-recall-burn-risk. Based on FDA recall #Z-0237-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0237-2023%22&limit=1).
The FDA announced on Oct. 24, 2022, that Whele LLC DBA Perch is recalling the Mighty Bliss Electric Heating Pad due to potential burn hazards. The voluntary Class I recall affects 12,140 units distributed nationwide through Amazon.com and Walmart.
How to tell if you have it
Brand: Perch
Product: Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24) Blue Electric Heating Pad
Model: MB-002
Lot codes: 210901, 211001
Quantity: 12,140 units
The hazard
According to the FDA, the products may have the potential to burn customers. The firm has received complaints of burns, mild shocks, and rashes or irritation.
Context
GovInfoNow's records show other recent recalls of similar products include Handy Solutions Neck & Should: Folded heating pad risks burns and fire (2026-02-18) and Medline Full Electric Low Lightweight Bed Recall: Fire Risk from Hand Pendant Overheating (2025-11-26). FDA's MAUDE device-report database lists 61 reports naming Mighty Bliss since October 2021, with 17 marked serious.
How to tell if you have this one
Check for the model MB-002 with blue color and size 20 x 24 inches. Affected units have UDI lots numbered 210901 through 211001.
Brand
Perch
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0237-2023 (October 24, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0237-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.