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FDA Medical Device Recalls (openFDA)

Ekos Corp: Lysus Transport Stand (infusion stand), part number 4896-003

Recall number
Z-0195-2007
Recalling firm
Ekos Corp
Product
Lysus Transport Stand (infusion stand), part number 4896-003
Status
Terminated
Initiated
2006-10-12
Posted
2006-11-16
Terminated
2006-11-20
Reason
Carts distributed without an additional caution label directly on the cart, alerting users to tipping hazard.
Root cause
Other
Action
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.
Quantity
84 carts
Distribution
Nationwide.
Lot, serial or model codes
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.
510(k) numbers
not on file
PMA numbers
not on file
Product code
FDX
Firm FEI
3001627457
Firm city
Bothell
Firm state
WA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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