ClearanceBrief
Recall Z-2176-2017 ยท KNT Tubes, Gastrointestinal (And Accessories)

AbbVie Inc.

AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

DateApr 27, 2017
StatusTerminated
Reason
Root causeUnder Investigation by firm
ActionOn April 27, 2017, firm sent letter (and response form) to customers, instructing them to inspect their inventory for affected lots and arrange a replacement kit to be delivered by AbbVie if a kit with missing components is discovered. Distributors were asked to notify their customers. Any returned affected product will be destroyed.
Quantity673 kits
DistributionNationwide, Albania, Austria, Australia, Belgium, Bulgaria, Canada, Switzerland, Czech Republic, Germany, Denmark, Estonia, Spain, Finland, France, Great Britain, Greece, Croatia, Hungary, Ireland, Italy, Japan, Korea, Luxembourg, Netherlands, Norway, Portugal, Romania, Russia, Saudi Arabia, Sweden,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K142793AbbVie PEG
AbbVie , Inc., Jan 14, 2015