American National Mfg Inc: Medical Device Recall in 2016 - (Recall #: Z-2605-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating pressure air flotation mattress.

Product Classification:

Class II

Date Initiated: July 11, 2016

Date Posted: August 31, 2016

Recall Number: Z-2605-2016

Event ID: 74737

Reason for Recall:

The Panacea Air Pro Mattress Control Unit is being recalled due to a firmware problem, which may result in the device not having the firmness range required.

Status: Terminated

Product Quantity: 31 units

Code Information:

Serial No. 9500051 sequential to 9500300.

Distribution Pattern:

Distributed to the US -- WI, OH, IL, TX, AZ, MD, IA, PA, CO, WA, ID, MN, LA, WY, and MS.

Voluntary or Mandated:

Voluntary: Firm initiated