RecallDepth
Class III Terminated

Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC 71399-8022-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ

Company
Akron Pharma, Inc.
Recall Initiated
August 4, 2022
Posted
August 24, 2022
Recall Number
D-1353-2022
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
30,325 bottles
Firm Location
Fairfield, NJ, United States

Reason for Recall

Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.

Distribution

Product was distributed to 6 distributors/wholesalers who may have further distributed the product.

Lot / Code Info

Lot#: AXA2014, Exp Feb-23; AXB2001, Exp Nov-22; AXB2002, AXB2003, AXB2004, AXB2005, AXB2006, AXB2007, AXB2008, AXB2009, AXB2010, AXB2011, Exp Dec-22; AXB2012, AXB2013, AXB2014, AXB2015, AXB2016, AXB2017, AXB2018, AXB2019, AXB2020, AXB2021, AXB2022, AXB2023, AXB2024, AXB2025, AXB2026, AXB2027, Exp Feb-23

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