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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