Product Number 3102071 Ceiling Bracket — Class II medical device recall Z-0326-2017
Terminated recall by Hill-Rom, Inc., reported 2016-11-09, distributed in MI, NC, OH, PA, WA. Ceiling Bracket 71 was shipped with a larger center hole. A potentially hazardous situation exists that if the
| Recall number | Z-0326-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom, Inc., Batesville, IN, United States |
| Recall initiated | 2016-08-09 |
| Classified | 2016-10-31 |
| Reported by FDA | 2016-11-09 |
| Terminated | 2017-03-24 |
| Distributed | MI, NC, OH, PA, WA |
| Countries outside the US | AU, SE |
| Quantity | 188 |
Product
Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likorall 200, 242, 243, 250, and LikoGuard L and XL.
Reason for recall
Ceiling Bracket 71 was shipped with a larger center hole. A potentially hazardous situation exists that if the Ceiling Bracket 71 with a larger center hole is used for a concrete ceiling Ultra System installation with the M8 screw and the safe working load is exceeded, the system could fall.
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-0326-2017. 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.