DrugJul 17, 2024
Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per recall — FDA D-0593-2024
Cross contamination with other products.
Class IIIFDA: OngoingZydus Pharmaceuticals (USA) Inc.
Latest records
Latest recalls — page 219
The newest recall records with useful source details are listed here.
DrugJul 17, 2024
Verapamil Hydrochloride Injection, USP 5 mg / 2mL(2.5 mg/mL), packaged as (a) 25x2 mL recall — FDA D-0592-2024
Cross contamination with other products.
Class IIIFDA: OngoingZydus Pharmaceuticals (USA) Inc.
VehicleJul 17, 2024
BMW structure recall — NHTSA campaign 24V534000
BMW of North America, LLC (BMW) is recalling certain 2018-2023 X3 sDrive30i, X3 xDrive30i, X3 M40i, and X3 M vehicles. The attachment for the interior cargo rail may become damaged in a…
structureBMW of North America, LLC
VehicleJul 12, 2024
Santa Fe control module software recall — NHTSA campaign 24V529000
Hyundai Motor America (Hyundai) is recalling certain 2024 Santa Fe vehicles. A software error in the transmission control unit may result in a vehicle roll away when the vehicle is in PARK.
control module softwareHyundai Motor America
DrugJul 10, 2024
Little Moon Essentials, Aching Head Rub recall — FDA D-0573-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 10, 2024
Integrity Products To the Moon Capsules, Horny Goat Weed, 1000 mg recall — FDA D-0586-2024
Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Class IFDA: OngoingIntegrity Products
DrugJul 10, 2024
Integrity Products RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg recall — FDA D-0585-2024
Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Class IFDA: OngoingIntegrity Products
DrugJul 10, 2024
Little Moon Essentials, Magical Muscle Oil recall — FDA D-0571-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 10, 2024
Little Moon Essentials, Dream Cream recall — FDA D-0574-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 10, 2024
Little Moon Essentials, Asana Kisser recall — FDA D-0577-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 10, 2024
SUN PHARMACEUTICAL INDUSTRIES Decitabine for Injection 50mg per vial, For intravenous recall — FDA D-0582-2024
CGMP Deviations: Out of Specification for Total Aerobic Microbial Count (TAMC) test for unfiltered bulk for decitabine for injection.
Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJul 10, 2024
The Harvard Drug Group LLC dba Major Venlafaxine Hydrochloride, extended-release capsules recall — FDA D-0584-2024
Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.
Class IIFDA: TerminatedThe Harvard Drug Group LLC dba Major Pharmaceuticals…
DrugJul 10, 2024
Little Moon Essentials, Clear Breeze Plus, Hand Sanitizer (Alcohol 65% v/v) Packaged as a) 2 recall — FDA D-0578-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 10, 2024
Little Moon Essentials, Vital Vapor Balm recall — FDA D-0575-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 10, 2024
Little Moon Essentials, Ass Kisser, Packaged as a) 0.5 OZ (14G) metal tin, UPC Code 6 73673 recall — FDA D-0576-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 10, 2024
Little Moon Essentials, Crampy Belly Rub (Camphor 1.1%), Packaged as a) 4 FL OZ (118ML) recall — FDA D-0572-2024
CGMP deviations
Class IIFDA: OngoingLittle Moon Essentials LLC
DrugJul 3, 2024
SinuFrin Decongestant (oxymetazoline HCl) Nasal Solution Nasal Decongestant, Decongestant recall — FDA D-0569-2024
Sub-potent Drug
Class IIIFDA: OngoingNeilmed Pharmaceuticals Inc.
DrugJul 3, 2024
Duloxetine Delayed-Release Capsules, USP, 30mg recall — FDA D-0568-2024
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the proposed interim limit.
Class IIFDA: TerminatedGolden State Medical Supply Inc.
DrugJul 3, 2024
Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile recall — FDA D-0564-2024
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Class IIFDA: OngoingPfizer Inc.
DrugJul 3, 2024
Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose Carpuject recall — FDA D-0565-2024
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Class IIFDA: OngoingPfizer Inc.
DrugJul 3, 2024
Zilretta recall — FDA D-0567-2024
Failed Dissolution Specifications - did not meet the acceptance criteria for IVR Level 3 testing at 9 months 2-8¿C followed by 6 weeks at 25¿C
Class IIFDA: OngoingPACIRA PHARMACEUTICALS Inc.
VehicleJul 2, 2024
CR-V markings recall — NHTSA campaign 24V508000
Honda (America Honda Motor Co.) is recalling certain 2024 CR-V vehicles. The tire identification number (TIN) is missing the four-digit date code. As such, these vehicles fail to comply…
markingsHonda (American Honda Motor Co.)
VehicleJul 1, 2024
Nissan Sentra windshield recall — NHTSA campaign 24V498000
Nissan North America, Inc. (Nissan) is recalling certain 2024 Nissan Sentra vehicles. The windshield may have air bubbles on the front lower driver's side, which can obscure the Vehicle…
windshieldNissan North America, Inc.
VehicleJun 28, 2024
General Motors tank recall — NHTSA campaign 24V491000
General Motors, LLC (GM) is recalling certain 2024 Chevrolet Colorado and GMC Canyon vehicles. The lock ring that secures the fuel pump to the fuel tank assembly may not have been fully…
tankGeneral Motors, LLC
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