FoodJun 29, 2022
Albertsons Companies Ready Meals PB & Trail Mix Snack recall — FDA F-1332-2022
Potential Salmonella contamination.
Class IFDA: TerminatedAlbertsons Companies LLC
June 2022 recalls — page 3
These records include useful source details for the selected month.
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
Medical DeviceJun 22, 2022
CRHF Cobalt Models loaded with CareLink SmartSync Device Manager application software recall — FDA Z-1267-2022
Telemetry error that may occur with Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).
Class IIFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 22, 2022
illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF recall — FDA Z-1259-2022
cybersecurity vulnerability
Class IIFDA: CompletedIllumina, Inc.
Medical DeviceJun 22, 2022
GE Healthcare CARESCAPE Central Station (CSCS) V2, Model numbers 2082278-001 and 2082279-001 recall — FDA Z-1265-2022
The CARESAPE Central Station (CSCS) V2 can shut down due to a potential power supply component failure. This can lead to loss of patient monitoring at the central station.
Class IIFDA: OngoingGE Healthcare, LLC
Medical DeviceJun 22, 2022
Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5 recall — FDA Z-1262-2022
Incorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of vision…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJun 22, 2022
Olympus URETERO-RENO FIBERSCOPE Model: URF-P6 recall — FDA Z-1263-2022
Incorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of vision…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJun 22, 2022
Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R recall — FDA Z-1264-2022
Incorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of vision…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJun 22, 2022
CRHF Crome Models loaded with CareLink SmartSync Device Manager application software recall — FDA Z-1268-2022
Telemetry error that may occur with Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).
Class IIFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 22, 2022
Tandem Diabetes Care t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM, and t:slim X2 Insulin recall — FDA Z-1258-2022
Insulin pumps may display unexpected fluctuation of the remaining battery life so ensure pump battery life does not fall below 25% remaining power. If the battery life drops to less than…
Class IIFDA: OngoingTandem Diabetes Care Inc.
FoodJun 22, 2022
Euphoria Trading Company, LLC Peanut Butter Classic Truffles are peanut butter ganache recall — FDA F-1316-2022
Potential contamination with Salmonella. Product contains Jif peanut butter.
Class IFDA: TerminatedEuphoria Trading Company, LLC.
FoodJun 22, 2022
Euphoria Trading Company, LLC Dark Chocolate Peanut Butter Meltaways are rectangular bars recall — FDA F-1317-2022
Potential contamination with Salmonella. Product contains Jif peanut butter.
Class IFDA: TerminatedEuphoria Trading Company, LLC.
FoodJun 22, 2022
Euphoria Trading Company, LLC Milk Chocolate Peanut Butter Meltaways are rectangular bars recall — FDA F-1318-2022
Potential contamination with Salmonella. Product contains Jif peanut butter.
Class IFDA: TerminatedEuphoria Trading Company, LLC.
FoodJun 22, 2022
Cedar Crest Specialties Net Wt recall — FDA F-1297-2022
Foreign material - plastic
Class IIFDA: TerminatedCedar Crest Specialties, Inc.
FoodJun 22, 2022
Butter Buds Food Ingredients recall — FDA F-1307-2022
Undeclared milk.
Class IFDA: TerminatedButter Buds Inc.
FoodJun 22, 2022
Deskins Wholesale Chocolate No-Bake,16 oz., Plastic Shell, 12-16 oz recall — FDA F-1308-2022
Products were made with peanut butter contaminated with Salmonella.
Class IFDA: TerminatedDeskins Wholesale, LLC
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.