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Forbes Rehab Services Inc

FDA Regulatory Profile

Forbes Rehab Services Inc has 1 FDA recall, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Forbes Rehab Services Inc" and its spelling variant "Forbes Rehab Services".

Latest recall
Z-0423-2022 · Class II · Oct 11, 2021
Latest inspection
Dec 20, 2024 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Forbes Rehab Services Inc's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Forbes Rehab Services Inc: FDA inspections per year 2017: 0 inspections020172018: 1 inspections120182019: 0 inspections020192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 0 inspections020232024: 1 inspections120242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202300000
202200000
202110010
202000000
201900000
201810000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent recalls

1 recall record on Oct 11, 2021.

NumberClassProductDate
Z-0423-2022Class IIAffected components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever…Oct 11, 2021

Recent FDA inspections

3 inspections from Jul 19, 2018 to Dec 20, 2024.

DateSiteProductClassificationFEI
Dec 20, 2024Mansfield, OHDevicesVoluntary Action Indicated (VAI)1000136418
Oct 27, 2021Mansfield, OHDevicesNo Action Indicated (NAI)1000136418
Jul 19, 2018Mansfield, OHDevicesVoluntary Action Indicated (VAI)1000136418
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1000136418Mansfield, OH3Dec 20, 2024

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FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.