Hill-Rom 1000 Bed — Class II medical device recall Z-1466-2013
Terminated recall by Hill-Rom, Inc., reported 2013-06-12, distributed nationwide. Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the
| Recall number | Z-1466-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom, Inc., Batesville, IN, United States |
| Recall initiated | 2013-04-15 |
| Classified | 2013-06-05 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2017-02-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, BH, BO, BR, BS, CA, CL, CN, CO, CR, EC, EG, FR, GH, HK, ID, IN, JO, JP, KR, KW, LB, MX, MY, PA, PK, PY, QA, SA, SG, TH, TW, VE, VN, ZA |
| Quantity | 8,737 devices |
| Serial numbers | J143AP0937 |
Product
Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the medical surgical area of the hospital.
Reason for recall
Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame.
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-1466-2013. 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.