DrugJan 3, 2024
CHLORTHALIDONE Tablets, USP, 25MG, 1000 Tablets recall — FDA D-0172-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
Latest records
Latest recalls — page 463
The newest recall records with useful source details are listed here.
DrugJan 3, 2024
Meloxicam Tablets, USP, 15 mg, 1000 Tablets per bottle recall — FDA D-0190-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Ipratropium Bromide and Albuterol Sulfate Inhalation Solution (0.5 mg/3 mg per 3 mL), 60 x 3 recall — FDA D-0161-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
NATURAL CHERRY HONEY HERB THROAT DROPS Ricola CherryHoney Herb Throat Drops recall — FDA D-0195-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
AMOXICILLIN for Oral Suspension USP, 400MG/5ML, 100ML (when reconstituted) recall — FDA D-0165-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Propranolol Hydrochloride Tablets, 20 mg, 100 Tablets per bottle recall — FDA D-0194-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
CARDINAL HEALTHCARE Lillow recall — FDA D-0187-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Terconazole Vaginal Suppositories, 80 mg, 3 Suppositories with Vaginal Applicator recall — FDA D-0198-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Meta Herbal Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack recall — FDA D-0206-2024
Marketed without an approved NDA/ANDA: Magnum XXL found to contain undeclared active pharmaceutical ingredient (API) - Sildenafil.
Class IFDA: OngoingMeta Herbal
DrugJan 3, 2024
Lisinopril and Hydrochlorothiazide Tablets USP, 10mg/12.5mg recall — FDA D-0188-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Fluticasone Propionate Nasal Spray USP, 50MCG per spray, 16 g net fill weight, 120 Metered recall — FDA D-0182-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Doxycycline Capsules, USP 100 mg, 50 Capsules recall — FDA D-0178-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Sertraline Tablets, USP 100 mg, 30 tablets per bottle recall — FDA D-0205-2024
CGMP Deviations: Inadequate line clearance which may result in a potential comingling of product.
Class IIFDA: OngoingLegacy Pharmaceutical Packaging LLC
DrugJan 3, 2024
CARDINAL HEALTHCARE Bumetanide Tablets, USP, 2 mg, 100 Tablets per bottle recall — FDA D-0171-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
ANORO ELLIPTA recall — FDA D-0160-2024
Failed Release Testing: Coarse Particle Mass for umeclidinium Out of Specification
Class IIIFDA: TerminatedGlaxoSmithKline LLC
DrugJan 3, 2024
TCP HRB ACQUISITON Brut Classic Antiperspirant & Deodorant recall — FDA D-0207-2024
Chemical contamination: Presence of benzene
Class IFDA: OngoingTCP HRB ACQUISITON LLC
DrugJan 3, 2024
SPIRIVA HANDIHALER recall — FDA D-0197-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
DrugJan 3, 2024
Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety recall — FDA D-0179-2024
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class IIFDA: TerminatedCARDINAL HEALTHCARE
Medical DeviceDec 27, 2023
Nurse Assist 0.9% Sodium Chloride: Product Name/Product Code: 10ML IV FLUSH STERILE recall — FDA Z-0512-2024
Sodium chloride irrigation USP, and sterile water for irrigation USP, that may be packaged inside kits, have the potential for a lack of sterility assurance, which could result in a…
Class IFDA: OngoingNurse Assist, LLC
Medical DeviceDec 27, 2023
Olympus Corporation of the Americas ACMI Roller Bar Electrodes bearing incorrect pouch label recall — FDA Z-0568-2024
Incorrect pouch labels, the contents within the mislabeled pouch were Roller Bar electrodes.
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceDec 27, 2023
Product Name/Product Code: CARDINAL: 100ML STERILE SALINE BOTTLE/1020, 100ML STERILE SALINE recall — FDA Z-0513-2024
Sodium chloride irrigation USP, and sterile water for irrigation USP, that may be packaged inside kits, have the potential for a lack of sterility assurance, which could result in a…
Class IFDA: OngoingNurse Assist, LLC
Medical DeviceDec 27, 2023
ResMed AirFit N20 Nasal Mask and User Guide recall — FDA Z-0539-2024
Masks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with magnets, and metallic…
Class IFDA: OngoingResMed Ltd.
Medical DeviceDec 27, 2023
Biomet Biolox Ceramic Option Head Zimmer 12/14 40mm -3, Item Number 00-8777-040-01 recall — FDA Z-0569-2024
One product complaint was received reporting that there was an incorrect adapter in the packaging. An adapter with neck length M/+0 was inside the product packaging, which should have…
Class IIFDA: OngoingBiomet, Inc.
Medical DeviceDec 27, 2023
Exactech Vantage Ankle System, Catalog Numbers: a) 350-21-04, b) 350-22-03 recall — FDA Z-0587-2024
Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Class IIFDA: OngoingExactech, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories