PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: June 7, 2017 Initiated: April 27, 2017 #Z-2176-2017

Product Description

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

Details

Recalling Firm
AbbVie Inc.
Units Affected
673 kits
Distribution
Nationwide, 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, Slovenia, Slovakia, Turkey
Location
North Chicago, IL

Frequently Asked Questions

What product was recalled?
AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.. Recalled by AbbVie Inc.. Units affected: 673 kits.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 7, 2017. Severity: Moderate. Recall number: Z-2176-2017.