Data Foundry

Medical device recalls 2022

Mighty Bliss Electric Heating Pad — Class I medical device recall Z-0236-2023

Ongoing recall by Whele LLC DBA Perch, reported 2022-11-30, distributed nationwide. The products may have the potential to burn customers. Firm has received complaints of burns, mild shocks, and

Recall numberZ-0236-2023
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmWhele LLC DBA Perch, Boston, MA, United States
Recall initiated2022-10-24
Classified2022-11-23
Reported by FDA2022-11-30
DistributedNationwide (US)
Quantity528,067
Lot numbers210108, 210109, 210110, 210111, 210201, 210202, 210203, 210204, 210301, 210302, 210303, 210304, 210305, 210306, 210307, 210308, 210309, 210310, 210401, 210402, 210403, 210405, 210406, 210407, 210501, 210502, 210801, 210802, 210803, 210804, 210805, 210806, 210901, 210902, 210903, 210904, 210905, 210906, 210907, 210908 and 32 more

Product

Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Blue Electric Heating Pad, MB-001

Reason for recall

The products may have the potential to burn customers. Firm has received complaints of burns, mild shocks, and rashes/irritation.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0236-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.