Z-2176-2017 Class II Terminated
FDA device recall Z-2176-2017 was initiated by AbbVie Inc. on April 27, 2017 and is designated Class II. The recall status is terminated (terminated July 9, 2019). Affected quantity: 673 kits.
Recall Details
- Product Type
- Devices
- Report Date
- June 7, 2017
- Initiation Date
- April 27, 2017
- Termination Date
- July 9, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 673 kits
Product Description
AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
Distribution Pattern
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
Code Information
Material/List number: 629100116 Lots: 32025245, 32054247, 32265215, 32335206, 32335336