FoodFeb 7, 2018
Hom'ade Foods Mary B's Butter Taste, 20 Biscuits, Value Pack, NET WT recall — FDA F-0692-2018
Products have the potential to be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedHom'ade Foods
Latest records
Latest recalls — page 1514
The newest recall records with useful source details are listed here.
DrugFeb 7, 2018
Medline All Purpose Instrument Tray, Sterile recall — FDA D-0277-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Industries Liberator Medical Supply Catheter Insertion Tray, Sterile, Single Use recall — FDA D-0296-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Industries Professional Hospital Supply Suture Removal Kit, Sterile, Single Use Only recall — FDA D-0313-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
A&H Focal MACA gold tablets, 6800 mg, 10-count bottle, labeling is in foreign language recall — FDA D-0571-2018
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Class IFDA: TerminatedA&H Focal Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0309-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Straight Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0291-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline GHS Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0281-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0318-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Incision Drainage Kit, Sterile, Single Use Only recall — FDA D-0305-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
A&H Focal STREE OVERLORD capsules, 3800 mg, 4-count bottle, labeling is in foreign language recall — FDA D-0564-2018
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Class IIFDA: TerminatedA&H Focal Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0280-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0307-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline General Purpose Tray, Sterile, Single Use Only recall — FDA D-0283-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline NICC Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0288-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Skin Staple Remover Kit, Sterile, Single Use Only recall — FDA D-0290-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
A&H Focal GERMANY NIUBIAN tablets, 3000mg, 10-count bottle, labeling is in foreign language recall — FDA D-0556-2018
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Class IFDA: TerminatedA&H Focal Inc.
DrugFeb 7, 2018
International Laboratories Clopidogrel Tablets, USP 75 mg, 30-count bottles recall — FDA D-0472-2018
LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles labeled as Clopidogrel tablets, USP 75 mg.
Class IFDA: TerminatedInternational Laboratories, LLC
DrugFeb 7, 2018
Medline Skin Biopsy Pack-LF, Sterile, Single Use Only recall — FDA D-0301-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Industries Medical Equipment Affiliates IV Start Kit, Sterile, Single Use Only recall — FDA D-0299-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
A&H Focal MAX MAN capsules, 3000 mg, 6-count bottle, labeling is in foreign language recall — FDA D-0565-2018
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Class IIFDA: TerminatedA&H Focal Inc.
DrugFeb 7, 2018
Medline General Purpose Tray, Sterile, Single Use Only recall — FDA D-0278-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Laceration Tray, Sterile, Single Use Only recall — FDA D-0279-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Anesthesia Kit, Single Use Only recall — FDA D-0306-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026244 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 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 categories