AbbVie Inc.: Medical Device Recall in 2017 - (Recall #: Z-2176-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 27, 2017

Date Posted: June 7, 2017

Recall Number: Z-2176-2017

Event ID: 77129

Reason for Recall:

Status: Terminated

Product Quantity: 673 kits

Code Information:

Material/List number: 629100116 Lots: 32025245, 32054247, 32265215, 32335206, 32335336

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

Voluntary or Mandated:

Voluntary: Firm initiated