Drug recall
(1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier…
FDA recall event 89562 · Class II · Hill-Rom, Inc.
Key facts
| Event ID | 89562 |
|---|---|
| Recall numbers | Z-0783-2022 |
| Recalling firm | Hill-Rom, Inc. |
| Product type | Devices |
| Products | (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhead lift. Intended for to make safe lifting of a patient… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Traverse rail carriage delivered with non-conforming screws are too short to ensure appropriate installation. There is potential that the screws are unable to secure the traverse rail appropriately… |
| Initiation date | Jan 14, 2022 |
| Report date | Mar 23, 2022 |
| Termination date | Nov 7, 2024 |
| City | Batesville |
| State | IN |
| Country | United States |
| FEI number | 1824206 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: