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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices/Home Healthcare

WHILL, INC.: WHILL Model C2 and Model F Powered Wheelchairs Recalled for Cyber Vulnerability

Agency Publication Date: April 24, 2026
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Summary

WHILL, INC. has recalled 7,009 battery-operated powered wheelchairs, including Model C2 and foldable Model F units. These devices were found to have a cyber vulnerability in their Bluetooth Low Energy (BLE) communication software that could potentially allow unauthorized access. Consumers are advised to contact their healthcare provider or the manufacturer for software update instructions and assistance.

Risk

A security weakness in the Bluetooth communication system could allow an unauthorized person to interfere with the device's wireless connectivity. This vulnerability was identified by the Cybersecurity and Infrastructure Security Agency (CISA) and requires a software update to prevent potential exploitation.

What You Should Do

  1. Check your WHILL Model C2 wheelchair for software versions earlier than HMI: 2.22 / MC: 1.13 and confirm if your serial number is listed in the recall (e.g., numbers starting with CB23, CB22, CB21, or CA21/22).
  2. Check your WHILL Model F wheelchair for software versions earlier than HMI: 2.23 / MC: 1.05 and confirm if your serial number is listed (e.g., numbers starting with FB12 or FA12).
  3. Verify the UDI/DI 04570072300019 on your device packaging or documentation to confirm it matches the recalled products.
  4. Contact your healthcare provider or WHILL, INC. directly for further instructions on how to receive the necessary software updates to fix the cyber vulnerability.
  5. For additional questions, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

📋Other Action

Software update and manufacturer contact

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: WHILL Model C2 Powered Wheelchair
Model / REF:
Model C2
UPC Codes:
04570072300019
Lot Numbers (76):
CB2307U25A0134
CB2307U25A0133
CB2307U25A0132
CB2307U25A0131
CB2307U25A0130
CB2307U25A0129
CB2307U25A0128
CB2307U25A0127
CB2307U25A0126
CB2307U25A0125
CB2307U25A0124
CB2307U25A0123
CB2307U25A0122
CB2307U25A0121
CB2307U25A0120
CB2307U25A0119
CB2307U25A0118
CB2307U25A0117
CB2307U25A0116
CB2307U25A0115
CB2207U25A0114
CB2207U25A0113
CB2207U25A0112
CB2207U25A0111
CB2207U25A0110
CB2207U25A0109
CB2207U25A0108
CB2207U25A0107
CB2207U25A0106
CB2207U25A0105
CB2207U25A0104
CB2207U25A0103
CB2207U25A0102
CB2207U25A0101
CB2207U25A0100
CB2207U25A0099
CB2207U25A0098
CB2207U25A0097
CB2207U25A0096
CB2207U25A0095
CB2207U25A0094
CB2207U25A0093
CB2207U25A0092
CB2207U25A0091
CB2207U25A0090
CB2207U25A0089
CB2207U25A0088
CB2207U25A0087
CB2107U25A0086
CB2107U25A0085
Product: WHILL Model F Powered Wheelchair (Foldable)
Model / REF:
Model F
UPC Codes:
04570072300019
Lot Numbers (195):
FB1203U2610192
FB1203U2610191
FB1203U2610190
FB1203U2610189
FB1203U2610188
FB1203U2610187
FB1203U2610186
FB1203U2610185
FB1203U2610184
FB1203U2610183
FB1203U2610182
FB1203U2610181
FB1203U2610180
FB1203U2610179
FB1203U2610178
FB1203U2610177
FB1203U2610176
FB1203U2610175
FB1203U2610174
FB1203U2610173
FB1203U2610172
FB1203U2610171
FB1203U2610170
FB1203U2610169
FB1203U2610168
FB1203U2610167
FB1203U2610166
FB1203U2610165
FB1203U2610164
FB1203U2610163
FB1203U2610162
FB1203U2610161
FB1203U2610160
FB1203U2610159
FB1203U2610158
FB1203U2610157
FB1203U2610156
FB1203U2610155
FB1203U2610154
FB1203U2610153
FB1203U2610152
FB1203U2610151
FB1203U2610150
FB1203U2610149
FB1203U2610148
FB1203U2610147
FB1203U2610146
FB1203U2610145
FB1203U2610144
FB1203U2610143

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98320
Status: Active
Manufacturer: WHILL, INC.
Sold By: authorized dealers; specialty retailers
Manufactured In: Japan
Units Affected: 7,009
Distributed To: Kansas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.