Lysus Transport Stand (infusion stand), part number 4896-003
FDA device recall Z-0195-2007 · posted 2006-11-16 · Terminated
Recall details
- Recalling firm
- Ekos Corp
- Reason for recall
- Carts distributed without an additional caution label directly on the cart, alerting users to tipping hazard.
- Action taken
- The firm''s representatives will visit the consignees, apply the caution label and provide a letter, dated October 2, 2006, to the consignee. The letter states that the representative applied the caution label to the cart and reminds consignees if the UPS is removed and the cart is loaded with pumps and bags there is a potential for the cart to tip.
- Root cause
- Other
- Status
- Terminated
- Product code
- FDX
- Quantity affected
- 84 carts
- Distribution
- Nationwide.
- Date initiated
- 2006-10-12
- Date posted
- 2006-11-16
- Date terminated
- 2006-11-20
- Location
- Bothell, WA
Monitor recalls programmatically
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