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
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Recalling FirmEdwards Lifesciences, LLC
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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