Spirit One A-C Powered Hospital Bed — Class II medical device recall Z-1555-2016
Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2016-05-04, distributed in AL, AZ, FL, GA, HI, IA, IL, KS…. Customer complaints associated with faulty brake system
| Recall number | Z-1555-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2015-07-02 |
| Classified | 2016-04-22 |
| Reported by FDA | 2016-05-04 |
| Terminated | 2017-03-24 |
| Distributed | AL, AZ, FL, GA, HI, IA, IL, KS, LA, MI, MN, MO, NE, NJ, OH, PA, SC, TN, TX |
| Countries outside the US | CA, GB |
| Quantity | 143 total |
| Serial numbers | 027772, 027773, 028003, 028216, 028654, 028655, 028656, 028657, 028659, 028660, 028661, 028663, 028664, 028788, 028793, 028834, 028835, 028836, 028837, 028838, 028839, 028840, 028841, 028842, 028843 and 112 more |
Product
Spirit One A-C Powered Hospital Bed
Reason for recall
Customer complaints associated with faulty brake system
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-1555-2016. 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.