WHILL Model F Wheelchair Recall Due to Cyber Vulnerability
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
WHILL, INC. is recalling 2324 units of the WHILL Model F powered wheelchair because of a cyber vulnerability in BLE communication, affecting products distributed in Kansas.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 14, 2026 and geographically references Kansas. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
WHILL Model F Recall
What Happened
WHILL, INC. is recalling the WHILL Model F powered wheelchair due to a cyber vulnerability in BLE communication, as identified by the CISA VDP program.
Which Products Are Affected
The affected products are WHILL Model F wheelchairs with software versions before HMI: 2.23 / MC: 1.05. A total of 2324 units are involved, with UDI/DI 04570072300019 and specific serial numbers listed in the recall notice. These units were distributed in Kansas.
What You Should Do
Consumers with affected products should contact WHILL, INC., as the recall was initiated via e-mail for further instructions on the voluntary recall.
Why This Matters
This recall is significant because it addresses a potential security risk in medical devices that could impact user safety; it is classified as Class I, indicating a high level of concern.
Source
FDA recall notice Z-1827-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (913 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to May 14, 2026.
Frequently Asked Questions
Common questions about this FDA recall.