Recall Z-1240-2015— Richard Wolf Medical Instruments Corp.
Class II · Terminated
Class II FDA medical device recall by Richard Wolf Medical Instruments Corp., initiated 2014-12-10, terminated 2017-07-31. FDA's recall record names no specific 510(k) clearance for this event. Product: The I-Cart is used to store, transport, and power video equipment used in medical procedures.. Reason: 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..
- Recalling firm
- Richard Wolf Medical Instruments Corp.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-12-10
- Terminated
- 2017-07-31
- Firm location
- Vernon Hills, IL, United States
Product description
The I-Cart is used to store, transport, and power video equipment used in medical procedures.
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.