AbbVie PEG Kit 20 FR
Reported: December 28, 2016 Initiated: November 22, 2016 #Z-0786-2017
Product Description
AbbVie PEG Kit 20 FR
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.
Details
- Recalling Firm
- AbbVie Inc.
- Units Affected
- 541 units
- Distribution
- U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.
- Location
- North Chicago, IL
Frequently Asked Questions
What product was recalled? ▼
AbbVie PEG Kit 20 FR. Recalled by AbbVie Inc.. Units affected: 541 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 28, 2016. Severity: Moderate. Recall number: Z-0786-2017.
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