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

Recall Z-0991-2019 — AVE 2 Birthing Bed

U.S. FDA — Device Enforcement · Czech Republic · 2019-01-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0991-2019
Date of alert
2019-01-07
Country / jurisdiction
Czech Republic
Risk level
Class II
Risk type
recall
Brand
Linet Spol. S.r.o.
Product category
device
Product type
Devices
Reported risk: LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cable breaking at the bed connection or the orange insulation of the power cable may fail causing a possible spark or possible exposure to a live conductor.
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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