FoodAug 7, 2024
Hoff & Pepper, Co LLC Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask recall — FDA F-1544-2024
Undeclared Allergen - Wheat
Class IIIFDA: TerminatedHoff & Pepper, Co LLC.
Latest records
Latest recalls — page 363
The newest recall records with useful source details are listed here.
FoodAug 7, 2024
Prophet Premium Blends Diamond Shruumz Gummies - Mega/Extreme Dose Watermelon recall — FDA F-1542-2024
Toxic levels of muscimol
Class IFDA: TerminatedProphet Premium Blends, LLC
FoodAug 7, 2024
Reser's Fine Foods Hill Country Fare Mustard Potato Salad refrigerated product is recall — FDA F-1543-2024
Mustard potato salad is being recalled due to plastic foreign material.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 7, 2024
Totally Cool Abilyn s Frozen Bakery Ice Cream Cake Vanilla & Chocolate 6" recall — FDA F-1547-2024
Possible contamination with Listeria monocytogenes
Class IIFDA: TerminatedTotally Cool, Inc.
FoodAug 7, 2024
Totally Cool Chipwich Vanilla Chocolate Chip Ice Cream Sandwich 4 fl oz recall — FDA F-1569-2024
Possible contamination with Listeria monocytogenes
Class IIFDA: TerminatedTotally Cool, Inc.
VehicleAug 7, 2024
Hyundai Sonata brake lights recall — NHTSA campaign 24V583000
Hyundai Motor America (Hyundai) is recalling certain 2024 Hyundai Sonata vehicles. The software for the brake lights may cause the brake lights to flash and not illuminate properly. As…
brake lightsHyundai Motor America
DrugAug 7, 2024
Ciprofloxacin ophthalmic solution USP, 0.3% as base, package in bottles: a) 10 mL recall — FDA D-0623-2024
Defective container: unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Class IIFDA: OngoingFDC Limited
DrugAug 7, 2024
Clonazepam Orally Disintegrating Tablets, USP (C-IV) 0.125mg, 60 tablets per carton recall — FDA D-0622-2024
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled as 0.125 mg instead of 0.25 mg. The blister strips inside the product carton reflect the correct strength…
Class IFDA: TerminatedEndo Pharmaceuticals, Inc.
DrugAug 7, 2024
Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, a).100-count bottle recall — FDA D-0619-2024
Failed Dissolution Specifications
Class IFDA: OngoingAmerisource Health Services LLC
DrugAug 7, 2024
Progesterone Injection, USP, 500 mg per 10 mL (50mg/mL), 10 mL Multiple-Dose Vial recall — FDA D-0624-2024
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
Class IIFDA: OngoingEugia US LLC
VehicleAug 6, 2024
Nissan Frontier headlights recall — NHTSA campaign 24V582000
Nissan North America, Inc. (Nissan) is recalling certain 2024 Nissan Frontier vehicles. The right-side headlight assemblies may have missing or illegible headlight aim markings, which can…
headlightsNissan North America, Inc.
VehicleAug 1, 2024
General Motors owners/service/other manual recall — NHTSA campaign 24V575000
General Motors, LLC (GM) is recalling certain 2024 Cadillac XT4 and Chevrolet Malibu vehicles. The vehicles may have the wrong owner's manual in the glove box. As such, these vehicles fail…
owners/service/other manualGeneral Motors, LLC
VehicleAug 1, 2024
Chrysler control module software recall — NHTSA campaign 24V572000
Chrysler (FCA US, LLC) is recalling certain 2021 Jeep Wrangler and Jeep Gladiator vehicles that were previously remedied under NHTSA recall number 23V-116. The software for the powertrain…
control module softwareChrysler (FCA US, LLC)
VehicleAug 1, 2024
BMW starter motor recall — NHTSA campaign 24V576000
BMW of North America, LLC is recalling certain 2019-2020 X5, X7, 2020 3 Series Sedan, X6, 2020-2021 7 Series Sedan, 2020 8 Series Convertible, 8 Series Coupe, and 2020 8 Series Gran Coupe…
starter motorBMW of North America, LLC
Medical DeviceJul 31, 2024
Perfusor Space Syringe Pump, Non-Wireless recall — FDA Z-2437-2024
Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may…
Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceJul 31, 2024
Siemens Medical Solutions USA Sensis Vibe systems with software version VD15B-Intended to be recall — FDA Z-2441-2024
If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceJul 31, 2024
Medtronic Neuromodulation A610 Clinician Programmer (CP) Software Application (app) with the recall — FDA Z-2427-2024
Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are limited to HEAD ONLY MRI eligibility.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceJul 31, 2024
Randox Laboratories RX Series CYSC- Cystatin C Reagent -Intended for in vitro diagnostic recall — FDA Z-2425-2024
Cystatin C Reagent marketed without a 510 (k)
Class IIFDA: OngoingRandox Laboratories Ltd.
Medical DeviceJul 31, 2024
Olympus Corporation of the Americas ESG-410 Electrosurgical Generator- In conjunction with recall — FDA Z-2415-2024
Electrosurgical Generators ESG-410 does not power on upon use, may result in delays in initiating treatment or prolonged surgery
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJul 31, 2024
Medtronic Xomed NIM Vital Nerve Monitoring systems recall — FDA Z-2409-2024
Potential for false negative response on the NIM Vital Nerve Monitoring System
Class IFDA: OngoingMedtronic Xomed, Inc.
Medical DeviceJul 31, 2024
Securitas Healthcare Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a recall — FDA Z-2418-2024
This is a risk that alarms will not be received by the Arial Wireless Nurse Call System and premature depletion of the battery.
Class IIFDA: OngoingSecuritas Healthcare LLC
Medical DeviceJul 31, 2024
Abbott Infinity 7, Implantable Pulse Generator, REF: 6662, SterileEO, Rx Only recall — FDA Z-2431-2024
Their is a potential that the implantable pulse generator replacement indicator and end of service date may be shorter than indicated in the product labeling potentially resulting in loss…
Class IIFDA: OngoingAbbott Medical
Medical DeviceJul 31, 2024
Perfusor Space Infusion Pump System recall — FDA Z-2433-2024
Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may…
Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceJul 31, 2024
Beckman Coulter Dxl 9000 Access Immunoassay Analyzer, Catalog #C11137 recall — FDA Z-2414-2024
The analyzers were built with nonconforming USB cables made with brass contacts instead of specified gold contacts. Brass contacts may corrode over time, leading to loss of internal…
Class IIFDA: OngoingBeckman Coulter, Inc.
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Recent recall archives
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September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 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 categories