AbbVie Inc.: Medical Device Recall in 2016 - (Recall #: Z-0786-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

AbbVie PEG Kit 20 FR

Product Classification:

Class II

Date Initiated: November 22, 2016

Date Posted: December 28, 2016

Recall Number: Z-0786-2017

Event ID: 75794

Reason for Recall:

AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.

Status: Terminated

Product Quantity: 541 units

Code Information:

AbbVie PEG Kit 20 Fr Product Code 62912-01-16 with lot numbers: 32025245, 32265215, 32335206, 32335336

Distribution Pattern:

U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.

Voluntary or Mandated:

Voluntary: Firm initiated