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Critical recall: Death or serious injury has been reported or is considered likely. Stop using this product now.

WHILL, INC. 2026-05-06 Health critical FDA
Health · FDA · Recall #FDA-Z-1826-2026

WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an… Recall

Issued May 6, 2026 · WHILL, INC.

In May 2026, WHILL, INC. recalled the WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Cyber vulnerability of BLE communication was found by CISA VDP program.

What you should do

  1. 1 Stop using WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact WHILL, INC. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
WHILL, INC.
Category
Health
Recall date
May 6, 2026
Units affected
Not reported
Sold at
US: Kansas
Recall number
FDA-Z-1826-2026
Made in
Japan
Issuing agency
FDA

In context

  • WHILL, INC. has 1 recall in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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