Medical Positioning Rapid Response HUT table — Class II medical device recall Z-2208-2014
Terminated recall by Medical Positioning Inc, reported 2014-08-20, distributed nationwide. Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg pos
| Recall number | Z-2208-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Positioning Inc, Kansas City, MO, United States |
| Recall initiated | 2014-07-10 |
| Classified | 2014-08-13 |
| Reported by FDA | 2014-08-20 |
| Terminated | 2017-01-03 |
| Distributed | Nationwide (US) |
| Quantity | 20 beds |
| Reason classes | device malfunction |
| Serial numbers | 802421, 802780, 802781, 802783, 802784, 802809, 802861, 802924, 802939, 802949, 802971, 803106, 803356, 803588, 803616, 803854, 803867, 803926, 804118 |
| Model numbers | 1017 |
Product
Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1017. Product Usage: Used to conduct syncope examinations.
Reason for recall
Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can cause the device to malfunction.
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-2208-2014. 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.