The I-Cart is used to store recalled over fire hazard
- Recall date
- December 10, 2014
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Richard Wolf Medical Instruments Corp. recalls The I-Cart is used to store, transport, and power video equipment used in medical procedures.
- Recall number
- Z-1240-2015
- FDA classification
- Class II
- Brand / firm
- Richard Wolf Medical Instruments Corp.
- Sold / distributed
- Nationwide
Why it was recalled
The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chassis.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
The I-Cart is used to store, transport, and power video equipment used in medical procedures.
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