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

Recall Z-1135-2022 — AC-powered adjustable medical beds with built-in electric DC actuators and controls.

U.S. FDA — Device Enforcement · Canada · 2022-04-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1135-2022
Date of alert
2022-04-11
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Umano Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00670482000487
Reported risk: There is a potential hazard of uninterrupted motion of the Motorized Wheel System due to the possible failure of a component in the electrical system of the Product.
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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