Ekos Corp Lysus Transport Stand (infusion stand), part number 4896-003 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Lysus Transport Stand (infusion stand), part number 4896-003
Brand
Ekos Corp
Lot Codes / Batch Numbers
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.
Products Sold
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.
Ekos Corp is recalling Lysus Transport Stand (infusion stand), part number 4896-003 due to Carts distributed without an additional caution label directly on the cart, alerting users to tipping hazard.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Carts distributed without an additional caution label directly on the cart, alerting users to tipping hazard.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026