FoodAug 26, 2020
HAVEN'S KITCHEN***GOLDEN TURMERIC TAHINI***NET WT 5oz recall — FDA F-1167-2020
Product is labeled as the wrong sauce, resulting in soy being undeclared on the label.
Class IFDA: TerminatedHaven'S Kitchen
Latest records
Latest recalls — page 982
The newest recall records with useful source details are listed here.
FoodAug 26, 2020
Natures Path Foods USA Gluten-Free Organic Mesa Sunrise Cereal USA, Nature's Path recall — FDA F-1254-2020
Undeclared Wheat and/or Barley.
Class IIFDA: TerminatedNatures Path Foods USA, Inc.
DrugAug 26, 2020
Calvin Scott & Company Topiramate 25mg Tabs White/round tablets, 10-count bags recall — FDA D-1520-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phendimetrazine Brown/Clear Capsules, 105 mg, 28-count bags recall — FDA D-1523-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Ultra Seal Extra Strength Headache Relief recall — FDA D-1513-2020
Failed Stability Specifications: Out-of-Specification (OOS) results for the Aspirin related compound Salicylic Acid was observed.
Class IIIFDA: TerminatedUltra Seal Corporation
DrugAug 26, 2020
Calvin Scott & Company Phentermine HCL White/Blue Speckled tablets, 37.5 mg recall — FDA D-1531-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phentermine HCL White/Blue Speck Tabs 37.5 mg, 28-count bags recall — FDA D-1530-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phentermine HCL Blue/White Capsules, 37.5 mg, 28-count bags recall — FDA D-1529-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Thyroid 1 Grain Tablets, 28-count bags recall — FDA D-1517-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phentermine HCL GrayYellow capsules, 15mg recall — FDA D-1526-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Lannett Company Prednisone Tablets, USP 2.5 mg, 100 tablets recall — FDA D-1508-2020
Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP 2.5 mg actually contained Prednisone Tablets, USP 10 mg
Class IIFDA: TerminatedLannett Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phentermine HCL Yellow Caps 30mg recall — FDA D-1527-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Thyroid Neutral Tabs 2 gr, 28-count tablets recall — FDA D-1519-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Hydrochlorothiazide 50mg tablets, 14-count bags recall — FDA D-1516-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Elitek (rasburicase) for injection, 7.5 mg vial recall — FDA D-1507-2020
Failed Stability Specifications: Out of Specification result for enzyme activity levels noted during routine stability testing.
Class IIFDA: OngoingSanofi-Aventis U.S. LLC
DrugAug 26, 2020
CareFusion 213 ChlroraPrep One-Step recall — FDA D-1511-2020
Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Class IFDA: TerminatedCareFusion 213, LLC
DrugAug 26, 2020
CHLORAPREP ONE-STEP BD ChloraPrep Clear 3 mL Applicators recall — FDA D-1509-2020
Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Class IFDA: TerminatedCareFusion 213, LLC
DrugAug 26, 2020
CareFusion 213 ChloraPrep With Tint recall — FDA D-1510-2020
Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Class IFDA: TerminatedCareFusion 213, LLC
DrugAug 26, 2020
Ultra Seal Pain Relief Maximum Strength recall — FDA D-1512-2020
Failed Stability Specifications: Out-of-Specification (OOS) results for the Aspirin related compound Salicylic Acid was observed.
Class IIIFDA: TerminatedUltra Seal Corporation
DrugAug 26, 2020
Calvin Scott & Company Phentermine HCL Blue Speckled tablets, 37.5 mg recall — FDA D-1532-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Thyroid 1 Gr tablets, 28-count bags recall — FDA D-1518-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phendimetrazine Yellow Tabs 35mg recall — FDA D-1522-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phentermine HCL Blue/Clear capsules, 30mg recall — FDA D-1528-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
DrugAug 26, 2020
Calvin Scott & Company Phentermine 15mg grey/Yellow Capsules, 28-count bags recall — FDA D-1525-2020
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Class IIFDA: TerminatedCalvin Scott & Company, Inc.
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026179 records · 4 categoriesSeptember 2026363 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 categories