FDAFDA · Food and drugs·Recall number Z-2176-2017
AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
Published June 7, 2017 · Recall initiated: April 27, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- AbbVie Inc.
- Distributor
- 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
- Lot
- Material/List number: 629100116 Lots: 32025245, 32054247, 32265215, 32335206, 32335336
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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