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Terminated

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

FDA Recall Z-0195-2007 · Posted 2006-11-16

Recalling FirmEkos Corp
Recall StatusTerminated
Product CodeFDX
Date Initiated2006-10-12
Date Terminated2006-11-20
Product Quantity84 carts

Reason for Recall

Carts distributed without an additional caution label directly on the cart, alerting users to tipping hazard.

Firm 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.

Root Cause

Other

Distribution Pattern

Nationwide.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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