Pressure IQ Evolve Mattress recall
Pressure IQ Evolve Mattress; Non-powered mattress replacement system. Intended for patients with medium to high risk for developing pressure ulcers…
Why was Pressure IQ Evolve Mattress recalled?
The firm received complaints regarding multiple mattresses were showing failures resulting in pressure ulcers.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All Pressure IQ Evolve mattresses equipped with the 60g pods, manufactured January 2012-December 2013.
- Product
- Pressure IQ Evolve Mattress; Non-powered mattress replacement system. Intended for patients with medium to high risk for developing pressure ulcers…
- Recalling firm
- Arjo Hospital Equipment AB
- Quantity
- 1,034 units
- Distribution
- Nationwide Distribution.
- Recall date
- March 18, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)