Recall Z-0195-2007
Ekos Corp · initiated October 12, 2006
Product
Lysus Transport Stand (infusion stand), part number 4896-003
Codes / lots: 060113010-001, 060113010-002, 060113010-003, 060113010-004, 060113010-005, 060113010-006, 060113010-007, 060113010-008, 060113010-009, 060113010-010, 060113010-011, 060113010-012, 060113010-013, 060113010-014, 060113010-015, 060324025-001, 060324025-002 The additional carts do not contain any type of serial number.
Reason for recall
Carts distributed without an additional caution label directly on the cart, alerting users to tipping hazard.
FDA-determined cause: Other
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.
Details
- Recall number
- Z-0195-2007
- Initiated
- October 12, 2006
- Posted by FDA
- November 16, 2006
- Terminated
- November 20, 2006
- Product code
- FDX – Endoscopic Cytology Brush
- Quantity
- 84 carts
- Distribution
- Nationwide.
- Recalling firm
- Ekos Corp, Bothell, WA