DrugJul 6, 2022
Daytrana recall — FDA D-1169-2022
Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.
Class IIFDA: OngoingNoven Pharmaceuticals Inc.
Latest records
Latest recalls — page 367
The newest recall records with useful source details are listed here.
DrugJul 6, 2022
Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles recall — FDA D-1163-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedPD-Rx Pharmaceuticals, Inc.
DrugJul 6, 2022
Losartan Potassium Tablets, USP 50 mg, 90 Tablets bottles recall — FDA D-1162-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedPD-Rx Pharmaceuticals, Inc.
DrugJul 6, 2022
Green Pharmaceuticals SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc recall — FDA D-1165-2022
Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.
Class IFDA: TerminatedGreen Pharmaceuticals, Inc.
VehicleJul 6, 2022
4Runner labels recall — NHTSA campaign 22V480000
Southeast Toyota Distributors, LLC (SET) is recalling certain 2020-2022 4Runner vehicles equipped with 20-inch Black Gunner Wheels. The load carrying capacity modification labels are…
labelsSoutheast Toyota Distributors, LLC
VehicleJul 1, 2022
Outback engine control module (ecu/ecm) recall — NHTSA campaign 22V473000
Subaru of America, Inc. (Subaru) is recalling certain 2022 Outback vehicles. The engine wiring harness may have been damaged, resulting in a loose electrical connection to the engine…
engine control module (ecu/ecm)Subaru of America, Inc.
VehicleJun 30, 2022
General Motors brake lights recall — NHTSA campaign 22V463000
General Motors (GM) has decided that certain 2022 model year Chevrolet Silverado, and GMC Sierra vehicles equipped with an accessory sport bar. The accessory sport bar contains a…
brake lightsGeneral Motors, LLC
DrugJun 29, 2022
SUN PHARMACEUTICAL INDUSTRIES Clonazepam Orally Disintegrating Tablets, USP, 0.125mg recall — FDA D-1155-2022
Failed Tablet/Capsule Specification; oversized tablet found in a bottle
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 29, 2022
Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton recall — FDA D-1154-2022
Lack of Assurance of Sterility: Manufacturing deviation which was reported due to a microbial excursion
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 29, 2022
ISOPROPYL ALCOHOL 70% ISOPROPYL ALCOHOL First aid antiseptic, 4 FL OZ (118 mL) bottle, Made recall — FDA D-1151-2022
Defective Container: Product may leak when squeezed or when not in an upright position determined to be due to defects in the bottle neck finish and insufficient tightening.
Class IIFDA: TerminatedVi-Jon, LLC
DrugJun 29, 2022
Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton recall — FDA D-1153-2022
CGMP Deviations: lots made with same active pharmaceutical ingredient (API) as lots that were rejected due to manufacturing issues that could cause the product to be out of specification…
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 29, 2022
Clonidine Transdermal System, USP 0.3 mg/day, 4 Patches (NDC 51862-455-01) per Carton recall — FDA D-1152-2022
Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.
Class IIFDA: TerminatedMayne Pharma Inc.
VehicleJun 24, 2022
Ford windshield recall — NHTSA campaign 22V451000
Ford Motor Company (Ford) is recalling certain 2022 Bronco and Ranger vehicles. The windshield may not have been properly bonded to the vehicle, which could allow it to detach during a…
windshieldFord Motor Company
VehicleJun 24, 2022
Nissan automatic transmission recall — NHTSA campaign 22V457000
Nissan North America, Inc. (Nissan) is recalling certain 2020-2022 Frontier and Titan vehicles. The transmission parking pawl may not engage when the vehicle is shifted into park, which can…
automatic transmissionNissan North America, Inc.
VehicleJun 24, 2022
Ford frame and members recall — NHTSA campaign 22V454000
Ford Motor Company (Ford) is recalling certain 2022 Lincoln Aviator and Ford Explorer vehicles. The engine rails may have been improperly heat-treated. As such, these vehicles fail to…
frame and membersFord Motor Company
VehicleJun 23, 2022
General Motors tank recall — NHTSA campaign 22V446000
General Motors, LLC (GM) is recalling certain 2022 Cadillac XT5, XT6, and GMC Acadia All-Wheel Drive (AWD) vehicles. The fuel tank rollover valve may not provide a proper seal in the event…
tankGeneral Motors, LLC
DrugJun 22, 2022
Washington Homeopathic Products Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C recall — FDA D-1127-2022
cGMP deviations
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugJun 22, 2022
SUN PHARMACEUTICAL INDUSTRIES medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL recall — FDA D-1143-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 22, 2022
HAND SANITIZER SAY GOODBYE TO GERMS Alcohol Antiseptic 80% Topical Non-Sterile Solution, 12 recall — FDA D-1149-2022
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Class IIFDA: TerminatedHand Sanitizer LLC
DrugJun 22, 2022
AMS Packaging Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML recall — FDA D-1148-2022
Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
Class IIFDA: OngoingAMS Packaging Inc.
DrugJun 22, 2022
Walmart Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles recall — FDA D-1157-2022
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain…
Class IFDA: CompletedWalmart Inc.
DrugJun 22, 2022
SUN PHARMACEUTICAL INDUSTRIES medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL recall — FDA D-1146-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 22, 2022
A.P. Nonweiler Alcohol Antiseptic 80%, Topical Solution, Hand Sanitizer, Non-Sterile recall — FDA D-1142-2022
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Class IIFDA: OngoingA.P. Nonweiler
DrugJun 22, 2022
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL recall — FDA D-1145-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
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Recent recall archives
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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