Recall Z-2890-2016— EKOS Corporation
Class II · Terminated
Class II FDA medical device recall by EKOS Corporation, initiated 2016-08-22, terminated 2016-12-30. FDA's recall record names no specific 510(k) clearance for this event. Product: The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and transport the EkoSonic Control Unit. The cart is designed with three poles to hold infusion pumps and fluid bags, a tray on which the EkoSonic Control unit sits and a base designed to hold an Uninterruptable Power Supply (UPS). The cart mounts on 4 wheels, two locking and two non-locking.. Reason: Casters on the EKOS carts may be missing washers which can cause premature wear and dislodgement of the casters/wheels leading to failure..
- Recalling firm
- EKOS Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-08-22
- Terminated
- 2016-12-30
- Firm location
- Bothell, WA, United States
Product description
The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and transport the EkoSonic Control Unit. The cart is designed with three poles to hold infusion pumps and fluid bags, a tray on which the EkoSonic Control unit sits and a base designed to hold an Uninterruptable Power Supply (UPS). The cart mounts on 4 wheels, two locking and two non-locking.
Reason for recall
Casters on the EKOS carts may be missing washers which can cause premature wear and dislodgement of the casters/wheels leading to failure.
Data sourced from openFDA. This site is unofficial and independent of the FDA.