Spirit Plus Bed — Class II medical device recall Z-2331-2016
Terminated recall by CHG Hospital Beds Inc, reported 2016-08-10, distributed nationwide. Stryker Medical is initiating a voluntary recall of the Spirit Select and Spirit Plus A-C powered hospital bed
| Recall number | Z-2331-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CHG Hospital Beds Inc, London, Canada |
| Recall initiated | 2016-06-28 |
| Classified | 2016-08-03 |
| Reported by FDA | 2016-08-10 |
| Terminated | 2017-06-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 4,308 units |
| Serial numbers | 029481, 029482, 029483, 029484, 029485, 029486, 029487, 029488, 029489, 029490, 029491, 029492, 029493, 029494, 029495, 029496, 029497, 029498, 029499, 029500, 029501, 029502, 029503, 029504, 029505 and 475 more |
| Model numbers | 5600 |
Product
Spirit Plus Bed, A-C Powered Hospital Bed
Reason for recall
Stryker Medical is initiating a voluntary recall of the Spirit Select and Spirit Plus A-C powered hospital beds due to reports of hi-lo actuators broken at the mount ends, which could cause the bed to unexpectedly lower resulting in patient injury.
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-2331-2016. 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.