Data Foundry

Medical device recalls 2018

Permobil powered wheelchairs — Class II medical device recall Z-3178-2018

Terminated recall by Permobil, Ab, reported 2018-09-26, distributed nationwide. This correction decision has been made because of a potential failure of one or both backrest bars providing b

Recall numberZ-3178-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPermobil, Ab, Timra, N/A, Sweden
Recall initiated2018-08-15
Classified2018-09-14
Reported by FDA2018-09-26
Terminated2021-05-03
DistributedNationwide (US)
Quantity3,134 units
Serial numbers2531000003, 2532000027, 2532000040, 2532000042, 2532000062, 2532000076, 2532001482, 2532001500, 2532001533, 2535002420, 2535002472, 2535002640, 2535002641, 2535002755, 2535002756, 2535002798, 2535002799, 2535002902, 2535002903, 2535002970, 2535003007, 2535003051, 2535003052, 2535003183, 2535003304 and 475 more
Model numbersC300PS, C350PS, C400PS, C500PS, M300PS

Product

Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Usage: The devices identified are intended to provide outdoor and indoor mobility to persons limited to a seated position that can operate a powered wheelchair.

Reason for recall

This correction decision has been made because of a potential failure of one or both backrest bars providing back support. If one or both back support telescoping bars fail the user could fall back leading to a potential injury.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3178-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.