Drug recall
Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
FDA recall event 70675 · Class II · Hill-Rom, Inc.
Key facts
| Event ID | 70675 |
|---|---|
| Recall numbers | Z-1820-2015 |
| Recalling firm | Hill-Rom, Inc. |
| Product type | Devices |
| Products | Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece. |
| Initiation date | Mar 2, 2015 |
| Report date | Jul 1, 2015 |
| Termination date | May 13, 2016 |
| 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: