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

Recall Z-0019-2015 — ArjoHuntleigh Contoura C1000 series beds are designed to accommodate patients weighing up to 990 lbs. (450 kg). Model C1000 is the basic bed. Model C1080 includes a weighing system and a power outlet for an ArjoHuntleigh approved mattress pump. Product Usage: The Contoura series bariatric beds

U.S. FDA — Device Enforcement · Sweden · 2014-03-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0019-2015
Date of alert: 2014-03-17
Country / jurisdiction: Sweden
Risk level: Class II
Risk type: recall
Brand: Arjo Hospital Equipment AB
Product category: device
Product type: Devices

Reported risk: There is a low but existing entrapment risk for a patient being treated on the Contoura 1000 and Contoura 1080 bariatric beds if they have a BMI < 40.

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.

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