Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AbbVie PEG Kit 20 FR Recalled by AbbVie Inc. Due to AbbVie is issuing an urgent field correction notification...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact AbbVie Inc. directly.
Affected Products
AbbVie PEG Kit 20 FR
Quantity: 541 units
Why Was This 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.
Where Was This Sold?
U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.
About AbbVie Inc.
AbbVie Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report