Recall Z-1820-2015— Hill-Rom, Inc.
Class II · Terminated
Class II FDA medical device recall by Hill-Rom, Inc., initiated 2015-03-02, terminated 2016-05-13. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Hill-Rom, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-03-02
- Terminated
- 2016-05-13
- Firm location
- Batesville, IN, United States
Product description
Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
Reason for recall
The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.
Data sourced from openFDA. This site is unofficial and independent of the FDA.