FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2802-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
Monthly breakdown
2015 recalls by month
Select a month to review the recall records reported during that period.
December 201593 records · 2 categoriesNovember 2015364 records · 2 categoriesOctober 2015140 records · 2 categoriesSeptember 2015269 records · 2 categoriesAugust 2015193 records · 2 categoriesJuly 2015660 records · 2 categoriesJune 2015111 records · 2 categoriesMay 2015295 records · 2 categoriesApril 2015719 records · 2 categoriesMarch 2015168 records · 2 categoriesFebruary 2015284 records · 2 categoriesJanuary 201543 records · 2 categories
2015 recalls — page 50
Records are ordered by the best available source date.
FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2794-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
FoodJul 15, 2015
Boba Direct Foil bags containing 2.2 lbs recall — FDA F-2807-2015
Bubble tea powders contain undeclared allergens.
Class IIFDA: TerminatedBoba Direct, Inc.
DrugJul 15, 2015
American Health Packaging Azithromycin tablets, USP 600mg recall — FDA D-1222-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
Apotex Losartan potassium tablets USP, 50 mg, 90-count bottle recall — FDA D-1214-2015
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
Class IIFDA: TerminatedApotex Inc.
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 10mg recall — FDA D-1227-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
Abrams Royal Pharmacy II CORTISOL-MC, 10mg CAP recall — FDA D-1231-2015
Failed Content Uniformity Specifications: Failed Uniformity of Dosage Units specifications.
Class IIIFDA: TerminatedAbrams Royal Pharmacy II, LLC
DrugJul 15, 2015
BioComp Pharma Maximum Strength Analgesic Thera-Gesic Pain Relieving Creme Relief from recall — FDA D-1233-2015
Subpotent Drug: menthol and methyl salicylate below specification
Class IIIFDA: TerminatedBioComp Pharma, Inc.
DrugJul 15, 2015
DEXTROSE 10% Dextrose Injection, USP, 250mL VIAFLEX Plastic bags recall — FDA D-1210-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
Apotex Losartan potassium tablets USP, 100 mg, 90-count bottle recall — FDA D-1213-2015
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
Class IIFDA: TerminatedApotex Inc.
DrugJul 15, 2015
Teva Pharmaceuticals USA Adrucil recall — FDA D-1089-2015
Presence of Particulate Matter: Black particulate matter was identified as aggregate of silicone rubber pieces from a filler diaphragm and fluorouracil crystals.
Class IFDA: TerminatedTeva Pharmaceuticals USA
DrugJul 15, 2015
Lactated Ringers Injection, USP, 250mL VIAFELX Plastic bags recall — FDA D-1211-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
DEXTROSE 5% Dextrose Injection, USP, 250mL VIAFLEX Plastic bags recall — FDA D-1209-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
Bupivacaine Hydrochloride Inj., USP, 0.5% (5 mg/mL), Preservative-Free, 30 mL Single Use recall — FDA D-1216-2015
Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Class IFDA: TerminatedHospira Inc.
DrugJul 15, 2015
American Health Packaging Amlodipine besylate tablets, USP 5mg recall — FDA D-1219-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 20mg recall — FDA D-1228-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Famotidine tablets, USP 20mg recall — FDA D-1225-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Amlodipine besylate tablets, USP 10 mg recall — FDA D-1220-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, in 250mL VIAFLEX Plastic bags recall — FDA D-1208-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
American Health Packaging Azithromycin tablets, USP 250mg recall — FDA D-1223-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 40mg recall — FDA D-1229-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
Hospira Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM recall — FDA D-1232-2015
Failed pH Specifications: 12 month stability testing
Class IIIFDA: TerminatedHospira Inc.
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 5mg recall — FDA D-1226-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Azithromycin tablets, USP 500mg recall — FDA D-1221-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
About the 2015 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.