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Terminated

Intravascular (IV) Administration Sets, Model No. 54IV12, 54IV22, 54IV32, MK2450, 54IV42, MK132, MK2156, MK2270, MK2292, MK2300, MK2374, MK2394, MK2508, MK2227

FDA Recall Z-0446-2016 · Posted None

Recall StatusTerminated
Product CodeDXO
Date Initiated2015-11-13
Date Terminated2016-07-15
Product Quantity147,350 units

Reason for Recall

Edward Lifesciences is recalling Intravascular (IV) Administration Sets due to the requirement of an additional FDA submission to support commercialization (clearance) of the devices.

Firm Action

An urgent product notification letter dated 11/13/15 was to customers to inform them that during an internal documentation review, the requirement of an additional FDA submission to support commercialization (clearance) of the devices was discovered. Customers are informed that the Edwards Lifesciences Intravascular (IV) Administration sets are temporarily unavailable for sale. Customers are informed that there is no increased risk to the patients' health or safety by using products in their current inventory and there is no impact to the IV sets included in pressure monitoring kits (with TruWave pressure transducer or VAMP system). Customers are informed that if they are in need of a substitute IV set, then to call customer service at (800) 424-3278. Customers instructed to respond to the customer response form by faxing it to (800) 422-9329.

Root Cause

Under Investigation by firm

Distribution Pattern

US

Official Source

View FDA Recall →

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

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