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
Latest records
Latest recalls — page 225
The newest recall records with useful source details are listed here.
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.
VehicleMar 28, 2024
General Motors lugs/nuts/bolts/studs recall — NHTSA campaign 24V237000
General Motors, LLC (GM) is recalling certain 2023 Chevrolet Colorado and GMC Canyon vehicles. The front wheel hub bolts may have been over-tightened and damaged during installation.
lugs/nuts/bolts/studsGeneral Motors, LLC
DrugMar 27, 2024
INFUMORPH 200 Infumorph recall — FDA D-0392-2024
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Class IIFDA: OngoingHikma Pharmaceuticals USA Inc.
DrugMar 27, 2024
Super Chill Products Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) recall — FDA D-0393-2024
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Class IFDA: TerminatedSuper Chill Products
VehicleMar 22, 2024
Ford tires recall — NHTSA campaign 24V223000
Ford Motor Company (Ford) is recalling certain 2023 Maverick and Bronco Sport vehicles. The tires may have been manufactured incorrectly, which may result in a loss of vehicle handling and…
tiresFord Motor Company
VehicleMar 22, 2024
Subaru of front passenger recall — NHTSA campaign 24V227000
Subaru of America, Inc. (Subaru) is recalling certain 2020-2022 Outback and Legacy vehicles. A capacitor in the sensors for the Occupant Detection System (ODS) may crack and short circuit,…
front passengerSubaru of America, Inc.
VehicleMar 22, 2024
Mustang hoses, lines/piping, and fittings recall — NHTSA campaign 24V220000
Ford Motor Company (Ford) is recalling certain 2024 Mustang vehicles equipped with 2.3L engines. The low-pressure fuel supply line may be damaged or cut, which can result in a fuel leak.
hoses, lines/piping, and fittingsFord Motor Company
VehicleMar 20, 2024
Telluride driveshaft recall — NHTSA campaign 24V214000
Kia America, Inc. (Kia) is recalling certain 2020-2024 Telluride vehicles. The intermediate shaft and right front driveshaft may not be fully engaged, which can result in vehicle roll away…
driveshaftKia America, Inc.
DrugMar 20, 2024
Optikem International TRP Natural Eyes Pink Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 recall — FDA D-0382-2024
Lack of Assurance of Sterility
Class IIFDA: OngoingOptikem International, Inc.
DrugMar 20, 2024
Micro Labs Telmisartan Tablets, USP 40mg recall — FDA D-0388-2024
Failed Stability Specifications: Out of specification for blend uniformity.
Class IIFDA: TerminatedMicro Labs Limited
DrugMar 20, 2024
Optikem International TRP Natural Eyes Red Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 recall — FDA D-0383-2024
Lack of Assurance of Sterility
Class IIFDA: OngoingOptikem International, Inc.
DrugMar 20, 2024
Optikem International TRP Natural Eyes Aging Eye Relief, Sterile Eye Drops, Homeopathic recall — FDA D-0381-2024
Lack of Assurance of Sterility
Class IIFDA: OngoingOptikem International, Inc.
DrugMar 20, 2024
Broncochem Cold & Tea recall — FDA D-0387-2024
Stability testing failures for one or two of the four active pharmaceutical ingredients among the finished drug products, i.e., Phenylephrine HCL, and/or Chlorpheniramine Maleate.
Class IIFDA: OngoingGlobal Corporation
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