Arjo Hospital Equipment AB: Medical Device Recall in 2015 - (Recall #: Z-1247-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Pressure IQ Evolve Mattress; Non-powered mattress replacement system. Intended for patients with medium to high risk for developing pressure ulcers while on a mattress.

Product Classification:

Class II

Date Initiated: September 1, 2014

Date Posted: March 18, 2015

Recall Number: Z-1247-2015

Event ID: 68235

Reason for Recall:

The firm received complaints regarding multiple mattresses were showing failures resulting in pressure ulcers.

Status: Terminated

Product Quantity: 1,034 units

Code Information:

All Pressure IQ Evolve mattresses equipped with the 60g pods, manufactured January 2012-December 2013.

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated