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

Recall Z-1315-2019 — Wombat Living, Size 3, Item Numbers: 953121-00, 953126-00, 953131-00, 953132-00, 935-135-00, 935136-00, 953211-00, 953221-00, 953222-00, 953225-00, 953226-00, 953231-001, 953232-00, 953236-00 Product Usage: Activity chair (wheelchair)

U.S. FDA — Device Enforcement · Denmark · 2019-03-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1315-2019
Date of alert
2019-03-28
Country / jurisdiction
Denmark
Risk level
Class II
Risk type
recall
Brand
R82 A/S
Product category
device
Product type
Devices
Reported risk: Firm received feedback form the market regarding breakage of the plastic joint which connects the back to the seat.
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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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.