RegWardenFDA facility compliance records
Recall

Class II — Forbes Rehab Services Inc

Recalling firmFORBES REHAB SERVICES INC.
Registered facilityFORBES REHAB SERVICES INC. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonWarning 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
ProductAffected 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)
Quantity3065 units
DistributionUS Nationwide distribution.
Initiated2021-10-11
Classified2021-12-28
Recall numberZ-0423-2022
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Forbes Rehab Services Inc (Z-0423-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/89134/

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