FoodAug 1, 2018
AMPI Sweet Type, Formula 521, Extra Grade, spray process recall — FDA F-1773-2018
Whey powder may have the potential to be contaminated with Salmonella.
Class IIFDA: TerminatedAMPI
Monthly breakdown
2018 recalls by month
Select a month to review the recall records reported during that period.
December 2018285 records · 4 categoriesNovember 2018342 records · 4 categoriesOctober 2018626 records · 4 categoriesSeptember 2018393 records · 4 categoriesAugust 2018569 records · 4 categoriesJuly 2018356 records · 4 categoriesJune 2018402 records · 4 categoriesMay 2018613 records · 4 categoriesApril 2018449 records · 3 categoriesMarch 2018523 records · 3 categoriesFebruary 2018612 records · 3 categoriesJanuary 2018290 records · 3 categories
2018 recalls — page 92
Records are ordered by the best available source date.
FoodAug 1, 2018
Prinova US Amino Life brand Product - L-Leucine Instant Sunflower 25 Kgs recall — FDA F-1657-2018
This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts…
Class IIIFDA: TerminatedPrinova US LLC
FoodAug 1, 2018
Prinova US Amino Life brand Product - BCAA 2:1:1 Instant Sunflower 25 Kgs recall — FDA F-1658-2018
This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts…
Class IIIFDA: TerminatedPrinova US LLC
FoodAug 1, 2018
Kerry Soy Honey Cluster 30 lb recall — FDA F-1787-2018
an ingredient in this product was manufactured during the time-frame and on the same piece of equipment that was associated with a salmonella outbreak.
Class IIFDA: TerminatedKerry Inc.
FoodAug 1, 2018
Papa John's Salads & Produce Superfood Salad Kit - 6.8 lbs recall — FDA F-1674-2018
It was discovered that a bulk salad kit was produced using the wrong components. Instead of cashews, peanuts were packed for the kit
Class IIFDA: TerminatedPapa John's Salads & Produce, Inc.
FoodAug 1, 2018
Biscomerica Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with recall — FDA F-1680-2018
Product labeling does not list milk in the contains statement; however milk is listed as in ingredient.
Class IIFDA: TerminatedBiscomerica, Inc.
FoodAug 1, 2018
Prinova brand Product - MRI Amintoten Strawberry Powder 25 Kgs recall — FDA F-1659-2018
This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts…
Class IIIFDA: TerminatedPrinova US LLC
FoodAug 1, 2018
H-E-B GROCERY COMPANY LP DBA HEB HEB Creamy Creations Vanilla Chocolate Cup 3 oz packaged in recall — FDA F-1669-2018
Potential to contain metal fragments
Class IIFDA: TerminatedH-E-B GROCERY COMPANY LP DBA HEB
FoodAug 1, 2018
Orca Bay Foods Consumer Packaging: WELLSLEY FARM WILD CAUGHT MAHI-MAHI LOINS recall — FDA F-1664-2018
Product is decomposed.
Class IIIFDA: TerminatedOrca Bay Foods LLC
FoodAug 1, 2018
Prinova brand Product - Reginator NV recall — FDA F-1660-2018
This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts…
Class IIIFDA: TerminatedPrinova US LLC
DrugAug 1, 2018
VALSARTAN AND HYDROCHLOROTHIAZIDE Solco Healthcare US Valsartan and Hydrochlorothiazide recall — FDA D-0972-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
DrugAug 1, 2018
Teva Pharmaceuticals USA Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 320 mg/25 mg recall — FDA D-0985-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingTeva Pharmaceuticals USA
DrugAug 1, 2018
VALSARTAN AND HYDROCHLOROTHIAZIDE Solco Healthcare US Valsartan and Hydrochlorothiazide recall — FDA D-0973-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
DrugAug 1, 2018
Testosterone Cypionate Injection, USP, 200 mg/mL recall — FDA D-0977-2018
Presence of Particulate Matter: organic and inorganic compounds detected in vials of product.
Class IIFDA: TerminatedSun Pharmaceutical Industries, Inc.
DrugAug 1, 2018
VALSARTAN AND HYDROCHLOROTHIAZIDE Solco Healthcare US Valsartan and Hydrochlorothiazide recall — FDA D-0975-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
DrugAug 1, 2018
MAJOR PHARMACEUTICALS Enalapril Maleate Tablets, USP, 2.5 mg, 100 Tablets (10 x 10) Unit recall — FDA D-0979-2018
Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the…
Class IIIFDA: TerminatedMAJOR PHARMACEUTICALS
DrugAug 1, 2018
VALSARTAN Solco Healthcare US Valsartan, USP, 40 MG Tablets, 30- count bottle recall — FDA D-0968-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
DrugAug 1, 2018
VALSARTAN Solco Healthcare US Valsartan, USP, 160 MG Tablets, 90-count bottles recall — FDA D-0970-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
DrugAug 1, 2018
VALSARTAN Solco Healthcare US Valsartan, USP, 80 MG Tablets, 90-count bottle recall — FDA D-0969-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
DrugAug 1, 2018
Teva Pharmaceuticals USA Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 320 mg/12.5 recall — FDA D-0984-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingTeva Pharmaceuticals USA
DrugAug 1, 2018
VALSARTAN Solco Healthcare US Valsartan, USP, 320 MG Tablets, 90-count bottle,Rx Only recall — FDA D-0971-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
DrugAug 1, 2018
Teva Pharmaceuticals USA Valsartan Tablets, USP 80 mg, 90-count bottle (NDC 0591-2168-19) recall — FDA D-0987-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingTeva Pharmaceuticals USA
DrugAug 1, 2018
Teva Pharmaceuticals USA Valsartan Tablets, USP 40 mg, 30-count bottle (NDC 0591-2167-30) recall — FDA D-0986-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingTeva Pharmaceuticals USA
DrugAug 1, 2018
VALSARTAN AND HYDROCHLOROTHIAZIDE Solco Healthcare US Valsartan and Hydrochlorothiazide recall — FDA D-0976-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingPrinston Pharmaceutical Inc.
About the 2018 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.