CLASS II ONGOING Device recall · Reported 5 Jan 2022 · FDA Enforcement Report
components are limited to the Monoprice charging cable recalled
Forbes Rehab Services is recalling components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever, distributed nationwide in the US. The recall was initiated on 11 Oct 2021 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0423-2022
- FDA event ID
- 89134
- Recalling firm
- Forbes Rehab Services, Mansfield, OH
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 11 Oct 2021
- FDA classified
- 28 Dec 2021
- Reported
- 5 Jan 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 11 Oct 2021 | Recall initiated by company | |
| 28 Dec 2021 | Classified by FDA | +78 days |
| 5 Jan 2022 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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
Product as listed by the FDA
Affected components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever Boost Cube charging brick components for the SoundPOD Bluetooth Speaker accessory to the ProSlate Speech Generation Devices (including Proslate 13: B398PS130; Proslate 10: B398PS100; Proslate 8: B398PS080; Proslate 4: B398PS040)
Where it was distributed
US Nationwide distribution.
Questions about this recall
Is components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever recalled?
Yes. Forbes Rehab Services recalled components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever on 11 Oct 2021. The recall is Class II and its status is Ongoing. Recall number Z-0423-2022.
Why was it recalled?
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
Which lots are affected?
All units
Where was it sold?
US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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