Panacea Air Pro Mattress Control Unit — Class II medical device recall Z-2605-2016
Terminated recall by American National Mfg Inc, reported 2016-08-31, distributed in AZ, CO, IA, ID, IL, LA, MD, MN…. The Panacea Air Pro Mattress Control Unit is being recalled due to a firmware problem, which may result in the
| Recall number | Z-2605-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | American National Mfg Inc, Corona, CA, United States |
| Recall initiated | 2016-07-11 |
| Classified | 2016-08-19 |
| Reported by FDA | 2016-08-31 |
| Terminated | 2017-01-17 |
| Distributed | AZ, CO, IA, ID, IL, LA, MD, MN, MS, OH, PA, TX, WA, WI, WY |
| Quantity | 31 units |
| Reason classes | software |
| Serial numbers | 9500051 |
| Model numbers | 5000 |
Product
Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating pressure air flotation mattress.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2605-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.