DrugJul 27, 2022
Nephron Sterile Compounding Center Ketamine HCl Injection, USP, 50 mg/5 mL (10 mg/mL*) recall — FDA D-1259-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
Latest records
Latest recalls — page 340
The newest recall records with useful source details are listed here.
DrugJul 27, 2022
Nephron Sterile Compounding Center Morphine Sulfate Injection, USP, 30 mg/30 mL (1 mg/mL) recall — FDA D-1266-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center 8.4% Sodium Bicarbonate Injection, USP, 4.2 g/50 mL recall — FDA D-1279-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Bupivacaine HCl 150 mg (3.0 mg/mL), Ketorolac recall — FDA D-1249-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Ropivacaine HCl 123 mg (2.46 mg/mL), Clonidine HCl 0.04 recall — FDA D-1278-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Amazon.com Ortiga mas Ajo Rey Reforzado con Omega 3, 6 y 9, is recall — FDA D-1296-2022
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Class IFDA: TerminatedAmazon.com, Inc.
DrugJul 27, 2022
Hydrogen Peroxide Topical Solution USP, 3%, 16 FL OZ (1 PT) 473 mL bottle, packaged as a) recall — FDA D-1244-2022
Cross Contamination With Other Products: Product is cross contaminated with low levels of isopropyl alcohol.
Class IIFDA: TerminatedVi-Jon, LLC
DrugJul 27, 2022
Amazon.com Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle recall — FDA D-1295-2022
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Class IFDA: TerminatedAmazon.com, Inc.
DrugJul 27, 2022
Nephron Sterile Compounding Center Succinylcholine Chloride Injection, USP, 200 mg/10 mL recall — FDA D-1281-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
VehicleJul 21, 2022
Tacoma vehicle latch anchor recall — NHTSA campaign 22V520000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2022-2023 Tacoma vehicles. One or more of the individual welds in the upper child seat anchors may be insufficient. As…
vehicle latch anchorToyota Motor Engineering & Manufacturing
VehicleJul 21, 2022
Nissan camera recall — NHTSA campaign 22V527000
Nissan North America, Inc. (Nissan) is recalling certain 2021-2022 Rogue, 2022 Frontier, Pathfinder, and Titan rental vehicles. When the Sirius XM subscription is set to "Not Subscribed,"…
cameraNissan North America, Inc.
VehicleJul 21, 2022
Toyota Motor Engineering & Manufacturing front passenger recall — NHTSA campaign 22V519000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2022 Rav4, Rav4 Hybrid, and Rav4 Prime vehicles. The front passenger seat may have been assembled with interference…
front passengerToyota Motor Engineering & Manufacturing
VehicleJul 21, 2022
Model S frontal air bag recall — NHTSA campaign 22V526000
Tesla, Inc. (Tesla) is recalling certain 2022 Model S vehicles. The front bumper carrier structure may alter the vehicle's crash detection, causing the front passenger air bag to deploy…
frontal air bagTesla, Inc.
DrugJul 20, 2022
Hydrogen Peroxide Topical Solution, USP, 32 fl. oz. (1 QT) 946 mL recall — FDA D-1191-2022
Labeling: Label Mix-Up-The primary label on the front of the bottles have Hydrogen Peroxide affixed to the front and back of the containers. However, the product inside the bottle is 70%…
Class IIFDA: TerminatedVi-Jon, LLC
DrugJul 20, 2022
Bryant Ranch Prepack Morphine Sulfate extended-Release Tablets, USP recall — FDA D-1187-2022
Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30…
Class IFDA: TerminatedBryant Ranch Prepack, Inc.
DrugJul 20, 2022
Latin Foods Market Arti King Refozado con Ortiga y Omega 3 Tablets, 100-count bottles, Hecho recall — FDA D-1284-2022
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and dexamethasone.
Class IFDA: TerminatedLatin Foods Market
DrugJul 20, 2022
Bryant Ranch Prepack Morphine Sulfate extended-Release Tablets, USP recall — FDA D-1188-2022
Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30…
Class IFDA: TerminatedBryant Ranch Prepack, Inc.
DrugJul 20, 2022
Testosterone Cypionate Injection, USP, 200mg/mL, CIII recall — FDA D-1190-2022
cGMP - Water leakage
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJul 20, 2022
Draximage MAA recall — FDA D-1189-2022
Lack of Assurance of Sterility: Out-of-specification test results obtained for Endotoxin testing.
Class IIFDA: TerminatedJubilant Draximage Inc.
VehicleJul 20, 2022
Volkswagen Group of fuel pump recall — NHTSA campaign 22V516000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019-2021 Audi Q8, and 2020-2021 Audi Q7 vehicles. A component inside the fuel pump may break, causing the fuel pump to…
fuel pumpVolkswagen Group of America, Inc.
VehicleJul 20, 2022
BMW fuel rail recall — NHTSA campaign 22V513000
BMW of North America, LLC (BMW) is recalling certain 2022 X1 xDrive 28i, X3 xDrive30i, and 228i Gran Coupe vehicles. The high-pressure fuel rail may crack and result in a fuel leak within…
fuel railBMW of North America, LLC
VehicleJul 20, 2022
Volkswagen Group of camera recall — NHTSA campaign 22V514000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 Golf GTI, Jetta GLI, Jetta NF, Arteon FL, Tiguan LWB, 2022 Taos, Jetta PA, Tiguan PA, 2021-2022 Atlas Cross Sport,…
cameraVolkswagen Group of America, Inc.
VehicleJul 19, 2022
Kia Motors spare tire recall — NHTSA campaign 22V509000
Kia Motors America (Kia) is recalling certain 2022 Sorento and Telluride vehicles. The vehicles may be equipped with an incorrect spare tire which, when installed, can impair the anti-lock…
spare tireKia Motors America
DrugJul 13, 2022
Mometasone Furoate, Topical Solution USP, 0.1 % Lotion, a) 30 ml-bottle (NDC 68462-385-37) recall — FDA D-1173-2022
Defective Container
Class IIIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026149 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categories