Hill-Rom, Inc. recalls Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
- Recall date
- March 2, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1820-2015
- FDA classification
- Class II
- Brand / firm
- Hill-Rom, Inc.
- Sold / distributed
- Worldwide Distribution-US (nationwide) including the states of MI & PA, and the countries of Belgium, England, Italy, Czech Republic, Turkey, Greece, Ireland, Scotland, Spain, and Lebanon.
Why it was recalled
The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
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