FDA Device recall Z-2605-2016
Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000
- FDA Device
- Class II
- terminated
- Published 2016-08-31
On 2016-08-31 the FDA classified a Class II recall of Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000 by American National Mfg, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2605-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-11 |
| Published | 2016-08-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | American National Mfg |
| Distribution | AZ, CO, IA, ID, IL, LA, MD, MN, MS, OH, PA, TX, WA, WI, WY |
Product
Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating pressure air flotation mattress.
Reason
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.
Identifiers
| code_info | Serial No. 9500051 sequential to 9500300. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2605-2016%22
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