FoodApr 3, 2024
Barsotti Organic Carrot Juice 16 oz recall — FDA F-1098-2024
Product was determined to be under processed.
Class IIFDA: TerminatedBarsotti Juice Company, Inc.
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 138
Records are ordered by the best available source date.
FoodApr 3, 2024
Pressery The label reads, "Golden Sunrise Cold Pressured Juice Carrot recall — FDA F-1095-2024
Bottle of juice was found at the store level with the incorrect sku label.
Class IIIFDA: TerminatedPressery, LLC
FoodApr 3, 2024
Otis McAllister Product LAbeled in part: "Emerald River Premium Thai Jasmine recall — FDA F-1108-2024
Foreign object; piece of glass.
Class IIFDA: TerminatedOtis McAllister
VehicleApr 3, 2024
Volkswagen Group of front passenger recall — NHTSA campaign 24V251000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2023 Audi S5 Cabriolet, A4 Allroad, Q5 Sportback, A3 Sedan, S5 Sportback, SQ7, TT Coupe, TT Roadster, RS5 Sportback, 2024…
front passengerVolkswagen Group of America, Inc.
DrugApr 3, 2024
SCA Pharmaceuticals fentaNYL 200 mcg/100 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride recall — FDA D-0397-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals PHENYLephrine HCl 500 mcg/5 mL in 0.9% Sodium Chloride Injection recall — FDA D-0416-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals PHENYLephrine HCl 500 mcg/5 mL in 0.9% Sodium Chloride Injection recall — FDA D-0415-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals HYDROmorphone HCl 30 mg/30mL in 0.9% Sodium Chloride Injection recall — FDA D-0409-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride Injection recall — FDA D-0405-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals fentaNYL 500 mcg/100 mL, Bupivacaine HCl 0.075% in 0.9% Sodium Chloride recall — FDA D-0401-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals PHENYLephrine HCl 1000 mcg/10 mL in 0.9% Sodium Chloride Injection recall — FDA D-0414-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals fentaNYL 200 mcg/100 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride recall — FDA D-0398-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals HYDROmorphone HCl 25 mg/25 mL in 0.9% Sodium Chloride Injection recall — FDA D-0408-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals PHENYLephrine HCl 800 mcg/10 mL in 0.9% Sodium Chloride Injection recall — FDA D-0420-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL recall — FDA D-0404-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals PHENYLephrine HCl 800 mcg/10 mL in 0.9% Sodium Chloride Injection recall — FDA D-0421-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals fentaNYL 500 mcg/100 mL, Bupivacaine HCl 0.04% in 0.9% Sodium Chloride recall — FDA D-0400-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection recall — FDA D-0403-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals PHENYLephrine HCl 400 mcg/10 mL in 0.9% Sodium Chloride Injection recall — FDA D-0418-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals HYDROmorphone HCl 10 mg/50 mL in 0.9% Sodium Chloride Injection recall — FDA D-0407-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals fentaNYL 1,250 mcg/25 mL Injection recall — FDA D-0402-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugApr 3, 2024
SCA Pharmaceuticals fentaNYL 100 mcg/50 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride recall — FDA D-0399-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
VehicleApr 2, 2024
Santa Fe back over prevention software recall — NHTSA campaign 24V246000
Hyundai Motor America (Hyundai) is recalling certain 2024 Santa Fe vehicles. The rearview camera image may be obstructed by a trailer parking assist message. As such, these vehicles fail to…
back over prevention softwareHyundai Motor America
VehicleApr 1, 2024
Forte lower arm recall — NHTSA campaign 24V244000
Kia America, Inc. (Kia) is recalling certain 2023 Forte vehicles. The right front lower control arm may have been improperly welded, which can cause it to fail.
lower armKia America, Inc.
About the 2024 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.