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

Recall Z-2399-2016 — Invacare¿ Bariatric Bed w/o mattress & rails, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.

U.S. FDA — Device Enforcement · United States · 2016-03-15 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2399-2016
Date of alert: 2016-03-15
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Invacare Corporation
Product category: device
Product type: Devices

Reported risk: The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. They discovered that the Junction Box may omit sparks which could result in a fire in the presence of flammable materials.

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-2399-2016 — Invacare¿ Bariatric Bed w/o mattress & rails, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.

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