Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0005-2018 — Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR

U.S. FDA — Device Enforcement · Sweden · 2017-09-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0005-2018
Date of alert
2017-09-01
Country / jurisdiction
Sweden
Risk level
Class II
Risk type
recall
Brand
Permobil, Ab
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
43407264
Reported risk: There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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