Use cautionMedical device recall · FDA · Published October 11, 2021
Forbes Rehab Services: Monoprice charging cable and iClever Boost Cube fire risk
Forbes Rehab Services recalls Monoprice charging cables and iClever Boost Cube chargers that may cause fire or electric shock if damaged or used with moisture. Affected units include specific SoundPOD Bluetooth Speaker accessories for ProSlate speech devices.
Warning Added: Using damaged cables or chargers, or charging when moisture is present, can cause fire, electric shock, injury, or damage to Speech Generating Device or other property
“Forbes Rehab Services: Monoprice charging cable and iClever Boost Cube fire risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61699-forbes-rehab-services-monoprice-charging-cable-and-iclever-boost-cube. Based on FDA recall #Z-0423-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0423-2022%22&limit=1).
The Food and Drug Administration announced on Oct. 11, 2021, that Forbes Rehab Services Inc is recalling Monoprice charging cables and iClever Boost Cube charging bricks due to fire and electric shock hazards. The agency issued recall number Z-0423-2022 for the voluntary Class II action.
The FDA stated that using damaged cables or chargers, or charging when moisture is present, can cause fire, electric shock, injury, or damage to Speech Generating Device or other property. The record does not report specific incidents or injuries.
Context
GovInfoNow's records show the brand has been involved in other recent recalls of similar products, including a Therabody Theragun G4 PRO Charger fire risk recall on June 23, 2026, and Medline Full Electric Low Lightweight Bed recalls regarding hand pendant overheating on Nov. 26, 2025.
How to tell if you have this one
Check for Monoprice charging cables with Product #4867 or 24W iClever Boost Cube chargers. Affected units are for SoundPOD Bluetooth Speaker accessories on ProSlate speech devices (models B398PS130, B398PS100, B398PS080, B398PS040).
Brand
Forbes Rehab Services
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check for Damage
Inspect cables and chargers for signs of damage or moisture exposure.
Discontinue Use
Stop using damaged or wet chargers immediately to prevent fire or electric shock.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-0423-2022 (October 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0423-2022 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.