FoodDec 13, 2023
FreshPoint Bix Produce Company Mixed Fruit Cup, clam-shell container recall — FDA F-0667-2024
Potential Salmonella contamination.
Class IFDA: TerminatedFreshPoint Bix Produce Company, LLC
December 2023 recalls — page 11
These records include useful source details for the selected month.
FoodDec 13, 2023
Market Cuts 1 lb Pineapple Spear 1 Pound clamshell UPC recall — FDA F-0610-2024
salmonella
Class IFDA: TerminatedMarket Cuts LLC
FoodDec 13, 2023
FoodDec 13, 2023
FreshPoint Bix Produce Company Bix Produce Mixed Fruit with Grapes products containing recall — FDA F-0669-2024
Potential Salmonella contamination.
Class IFDA: TerminatedFreshPoint Bix Produce Company, LLC
FoodDec 13, 2023
Hilltop Meadow Farm 1 lb., 1.15 lb, 2.5 lb., and 5 lb recall — FDA F-0502-2024
Potential contamination with Listeria monocytogenes
Class IFDA: TerminatedHilltop Meadow Farm
FoodDec 13, 2023
Market Cuts 40 oz Combo Tray Fruit Small 40 Ounce tray UPC recall — FDA F-0614-2024
salmonella
Class IFDA: TerminatedMarket Cuts LLC
FoodDec 13, 2023
Freshpoint Of Southern Ca Whole cantaloupe 3ct and 6ct brand name Imperial Fresh recall — FDA F-0601-2024
The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Class IFDA: TerminatedFreshpoint Of Southern Ca
FoodDec 13, 2023
FreshPoint Dallas Whole cantaloupe 3ct and 6ct recall — FDA F-0617-2024
TruFresh in Nogales, AZ issued a voluntary recall of its Malichita, Mexico-sourced whole cantaloupe sold in the United States for potential Salmonella contamination.
Class IFDA: TerminatedFreshPoint Dallas
VehicleDec 13, 2023
Volkswagen Group of onboard recall — NHTSA campaign 23V842000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2022-2024 RS e-tron GT, e-tron GT, Q4 e-tron Sportback, Q4 e-tron, 2020-2021 Audi A8, 2019-2024 e-tron Quattro, 2020-2024…
onboardVolkswagen Group of America, Inc.
DrugDec 13, 2023
Novartis Pharmaceuticals SANDIMMUNE Oral Solution recall — FDA D-0144-2024
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals
Class IFDA: OngoingNovartis Pharmaceuticals Corporation
DrugDec 13, 2023
Ondansetron Injection, USP, 4 mg/2 mL (2 mg/mL), 2 mL per vial recall — FDA D-0146-2024
Failed pH Specifications
Class IIFDA: CompletedBaxter Healthcare Corporation
DrugDec 13, 2023
STAQ Pharma ROPivacaine HCl 0.2% PF in Sodium Chloride 1,000 mg/500 mL (2 mg per mL) recall — FDA D-0147-2024
STAQ Pharma Inc. received consumer complaints related to leaking bags and other potential bag concerns. Upon investigation, they determine the source of the issue was with the bag…
Class IIFDA: CompletedSTAQ Pharma, Inc.
DrugDec 13, 2023
SUGARMDS Dr. Ergin's SugarMD, ADVANCED GLUCOSE SUPPORT Capsules, Dietary Supplement, helps recall — FDA D-0138-2024
MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with metformin and glyburide
Class IFDA: OngoingSUGARMDS LLC
DrugDec 13, 2023
Trospium Chloride Extended-Release Capsules, 60 mg, 30 Capsules per bottle recall — FDA D-0139-2024
Failed Tablets/Capsules specifications; missing/broken/extra tablets within the capsules
Class IIFDA: OngoingPadagis US LLC
VehicleDec 12, 2023
Tesla autonomous/self driving software recall — NHTSA campaign 23V838000
Tesla, Inc. (Tesla) is recalling 2012-2023 Model S, 2016-2023 Model X, 2017-2023 Model 3, and 2020-2023 Model Y vehicles equipped with all versions of Autosteer leading up to the version(s)…
autonomous/self driving softwareTesla, Inc.
VehicleDec 7, 2023
XC90 critical fasteners recall — NHTSA campaign 23V827000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2015-2024 XC90 vehicles. The second-row seat belt buckle and lower belt anchor bolts may not be tightened properly.
critical fastenersVolvo Car USA, LLC
Medical DeviceDec 6, 2023
Aizu Olympus Co GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE recall — FDA Z-0417-2024
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of…
Class IIFDA: OngoingAizu Olympus Co., Ltd.
Medical DeviceDec 6, 2023
Edwards Lifesciences Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85 recall — FDA Z-0409-2024
Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Class IIFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceDec 6, 2023
Edwards Lifesciences FloTrac Sensor with Vamp System, REF: MHD6AZ, MHD6AZ5 , MHD6C502 recall — FDA Z-0412-2024
Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Class IIFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceDec 6, 2023
Edwards Lifesciences TruWave with Vamp System Pressure monitoring set, REF: PXAVMP(3cc)/VAMP recall — FDA Z-0414-2024
Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Class IIFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceDec 6, 2023
Edwards Lifesciences FloTrac Sensor, REF: MHD8 & MHD85,MHD6R5, MHD8R, MHD8R5, MHD8S recall — FDA Z-0411-2024
Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Class IIFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceDec 6, 2023
Edwards Lifesciences TruWave Pressure monitoring set, REF: PX212: cc/12 in (30cm), PX260 recall — FDA Z-0413-2024
Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Class IIFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceDec 6, 2023
Abbott Molecular Alinity m HCV AMP kit, List (REF) Numbers: a) 08N50-095 and b) 08N50-090 recall — FDA Z-0407-2024
Abbott has received reports of an increase in reactive negative controls and false positive results in patient samples when using the Identified Lots of Alinity m HCV AMP Kit.
Class IIFDA: OngoingAbbott Molecular, Inc.
Medical DeviceDec 6, 2023
Edwards Lifesciences Acumen IQ Sensor with VAMP System, REFs: AIQS6AZ & AIQS6AZ5, STERILEEO recall — FDA Z-0410-2024
Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Class IIFDA: OngoingEdwards Lifesciences, 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.