Product Recalls: May 14, 2025 – June 18, 2025
Health Letter, July 2025
Note: Never stop taking a drug that appears on the product recall list without first talking to your doctor or pharmacist. Most recalls are limited to a single manufacturer and may not be related to the version of a particular drug you are taking. If a recall does relate to the version of the drug you are taking, you should not stop taking the drug until you discuss an alternative treatment with your doctor or pharmacist.
For Class 1 recalls, there is a potential for serious injury or death.
For Class 2 recalls, there is a potential for serious adverse events but a lower chance of the drug causing serious injury or death than in a Class 1 recall.
CLASS I
CLASS II
carvedilol tablets; 3.125, 6.25, 12.5 or 25 mg; 100- or 500-count bottle. Manufactured by: Glenmark Pharmaceuticals Ltd. Lot #: 19231450, exp. date: Mar-25; Lot #: 19233345, exp. date: Jul-25; Lot #: 19234275, exp. date: Sep-25; Lot #: 19240280, exp. date: DEC-25; Lot #: 19231450, 19231464, 19231471 or 19231493, exp. date: Mar-25; Lot #: 19232083 or 19232103, exp. date: Apr-25; Lot #: 19232658, exp. date: Jun-25; Lot #: 19233328, 19233343, 19233344 or 19233345, exp. date: Jul-25; Lot #: 19234275, exp. date: Sep-25; Lot #: 19234843 or 19235039, exp. date: Nov-25; Lot #: 19240280 or 19240296, exp. date: Dec-25; Lot #: 19231618, exp. date: Mar-25; Lot #: 19232064, exp. date: Apr-25; Lot #: 19232324, exp. date: May-25; Lot #: 19233369, exp. date: Jul-25; Lot #: 19234162, exp. date: Sep-25; Lot #: 19240543, exp. date: Jan-26; Lot #: 19231174, 19231199 or 19231164, exp. date: Feb-25; Lot #: 19231517, 19231527, 19231566, 19231568, 19231595, 19231618, 19231634, 19231638 or 19231448, exp. date: Mar-25; Lot #: 19232043, 19232051, 19232064, exp. date: Apr-25; Lot #: 19232322, 19232324, 19232365, 19232380 or 19232389, exp. date: May-25; Lot #: 19232736, 19232743, 19232746, 19232756 or 19232757, exp. date: Jun-25; Lot #: 19233369, 19233371, 19233405 or 19233416, exp. date: Jul-25; Lot #: 19234162, 19234183, 19234192, 19234204, 19234223, 19234243, 19234263, 19234165 or 19234242, exp. date: Sep-25; Lot #: 19234743, 19234774 or 19234993, exp. date: Nov-25; Lot #: 19240223, 19240203, 19240211, 19240214, 19240247, 19240249, 19240272 or 19240319, exp. date: Dec-25; Lot #: 19240543, exp. date: Jan-26; Lot #: 19231899, 19231922, 19231927, 19231967 or 19231979, exp. date: Apr-25; Lot #: 19232226, 19232234, 19232265 or 1923227, exp. date: May-25; Lot #: 19232758, 19232759, 19232762 or 19232788, exp. date: Jun-25; Lot #: 19231107, 19231114 or 19231152, exp. date: Feb-25; Lot #: 19234866, exp. date: Jan-26.
celecoxib capsules, 200 mg, 500-count bottle or 5×10 unit dose per carton. Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division) or Manufactured for: AvKARE. Batch #: 2405014780, exp. date: Sep. 30, 2027; Lot # 47881, exp. date: 05/31/2026.
chlorthalidone tablets, 25 mg, 50 Tablets (5×10) unit dose cards per carton. Manufactured for: AvKARE. Lot #: 47947, exp. date: 05/31/2026.
fluoxetine tablets, 20 mg, 30-count bottle or 28-count carton. Manufactured by: TORRENT PHARMACEUTIALS LTD. Lot #: BDX6K001, exp. date: 06/30/2025; Lot #: BDX6K001, exp. date: 06/30/2025.
indomethacin extended-release capsules, 75 mg, 100-count bottle or 30 capsules (3 x 10 blister cards). Manufactured by: KVK-Tech, Inc. or Distributed by: American Health Packaging. Lot #: 18400A, exp. date: 7/31/2027; Lot #: 1021950, exp. date: 11/30/2026.
phentermine hydrochloride capsules, 30 mg, 100-count bottle. Manufactured by: KVK-Tech, Inc. Lot #: 18350A or 18351A, exp. date: 6/30/2027.
theophylline (anhydrous) extended-release tablets, 600 mg, 100 tablets per bottle. Manufactured by: Glenmark Pharmaceuticals Limited. Lot #: 19234121 or 19234148, exp. date: Sep-30-25; Lot #: 19242881 or 19242899, exp. date: Jun-30-26.
For more information about the drug recalls listed above, please visit http://www.accessdata.fda.gov/scripts/ires/index.cfm.
CONSUMER PRODUCTS
For a list of recent recalls of consumer products, please visit the Consumer Product Safety Commission website at http://www.cpsc.gov/en/Recalls/.