FDA Device recall Z-1820-2015
Steriseal-Cannula Ophthalmic
- FDA Device
- Class II
- terminated
- Published 2015-07-01
On 2015-07-01 the FDA classified a Class II recall of Steriseal-Cannula Ophthalmic by Hill Rom, citing the metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1820-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-02 |
| Published | 2015-07-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hill Rom |
| Distribution | US |
Product
Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
Reason
The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.
Identifiers
| code_info | Product #s: 157400; 257400; 157500; 257500 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1820-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.