Device Recall
FDA•CRITICAL
Ivenix Infusion System LVP Software
Fresenius Kabi is recalling Ivenix Infusion System LVP software due to a potential battery-health reporting error that may cause pump shutdown.
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FDA•CRITICALB. Braun Spinal Needle Procedure KitsB. Braun is recalling various spinal needle procedure kits due to quality issues with the included Bupivacaine Hydrochloride injection.
3 products
FDA•CRITICALCheese Sauce MixThe Coffee Connexion is recalling cheese sauce mix products due to potential Salmonella contamination in a dry milk powder ingredient.
4 products
NHTSA•MODERATETesla Model 3, Model Y, Model S, Model X Rearview CameraTesla recalls Model 3, Y, S, X vehicles with delayed rearview camera image in reverse (software 2026.8.6).
NHTSA•MODERATEWinnebago Solis Liquid Propane HoseWinnebago is recalling 2026–2027 Solis RVs; LP hose may be incorrectly routed over exhaust heat shield, risking fire.
NHTSA•MODERATE2025 Utilimaster Velocity Cargo Capacity LabelShyft is recalling 2025 Utilimaster Velocity vehicles with incorrect cargo capacity labels.
FDA•CRITICALStoltzfus Family Farm Sour Cream and Onion Cheese CurdsStoltzfus Family Dairy is recalling 8-ounce Sour Cream and Onion cheese curds due to potential Salmonella contamination.
FDA•CRITICALSouthern Style Nuts Gourmet Hunter MixJohn B. Sanfilippo & Son is recalling Gourmet Hunter Mix due to potential Salmonella contamination.
6 products
FDA•CRITICALButter Parsley Bagel CrispsLegacy Bakehouse is recalling Butter Parsley Bagel Crisps due to potential Salmonella contamination from recalled milk powder.
3 products
FDA•CRITICALGuittard 72% Cacao Chocolate with Date Sugar WafersGuittard is recalling 25lb bulk containers of 72% Cacao Chocolate with Date Sugar Wafers due to potential Salmonella contamination.
FDA•MODERATEMy Wife's SlawMy Wife's Slaw is being recalled due to a lack of required regulatory safety inspections during the manufacturing process.
2 products
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, due to failed dissolution specifications.
NHTSA•MODERATE2026 Toyota 4Runner Load Capacity Label2026 Toyota 4Runner recalled for incorrect load capacity label that may lead to improper loading.
FDA•LOWBusulfan InjectionSagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.
FDA•MODERATEMarket of Choice Vegan Kale Caesar SaladMarket of Choice is recalling Vegan Kale Caesar Salad due to an undeclared sesame allergen in the Za'atar spice.
FDA•CRITICALKayserBett IDA Pediatric Care BedKayserBetten is recalling IDA pediatric care beds due to an entrapment risk if hand controls are not locked while the child is unattended.
NHTSA•MODERATEMercedes-Benz Infotainment Control UnitMercedes-Benz is recalling 2024–2026 AMG GT, C-Class, E-Class, SL, CLE, and GLC vehicles; infotainment unit may reset and blank the instrument panel display.
NHTSA•MODERATERam ProMaster Rear Bench Seat LegsBraun is recalling 2026 Ram ProMaster vehicles with rear bench seats missing two of four legs.
NHTSA•MODERATENew Flyer XE40 Speedometer IlluminationNew Flyer is recalling 2022 XE40 transit buses with speedometers that may not illuminate with headlights on.
NHTSA•MODERATEMercedes-Benz CLA 350 4MATIC and CLA 250+ Front Passenger Seat BeltMercedes-Benz recalls 2026 CLA 350 4MATIC and CLA 250+ front passenger seat belts that may remain locked and cannot extend.
- Equipment RecallNHTSA•MODERATEWaymo 5th and 6th Generation Automated Driving System
Waymo recalls 5th and 6th Gen ADS software that may drive vehicles into standing water on high-speed roads.
FDA•MODERATE...And KimchiOcinet is recalling ...And Kimchi in 30oz, 63oz, and 126oz sizes due to an undeclared fish allergen.
FDA•LOWPrimidone Tablets 250 mgAmerican Health Packaging is recalling Primidone Tablets 250 mg distributed nationwide due to potential cross-contamination with Acemetacin.
2 products
FDA•MODERATENephronex Vitamin B-Complex, Vitamin C & Folic Acid LiquidSafecor Health is recalling Nephronex oral liquid supplement due to foreign substance contamination from observed black particles.
FDA•CRITICALFiery Hot Seasoning (Reduced Salt)JCB Flavors is recalling 25 lb containers of Fiery Hot Seasoning (Reduced Salt) due to potential Salmonella contamination.
10 products
FDA•CRITICALa2 Platinum Premium Infant FormulaThe a2 Milk Company is recalling 31.7oz tins of a2 Platinum Premium infant formula due to potential Cereulide toxin contamination.
FDA•MODERATESecond Nature Keto Crunch Smart MixSecond Nature is recalling Keto Crunch Smart Mix due to undeclared cashews, pistachios, and dried cherries.
NHTSA•MODERATEGrand Design Lineage Seat BaseGrand Design is recalling 2025–2026 Lineage RVs with improperly tightened driver and passenger seat bases that may move in a crash.
- NHTSA•MODERATEGrand Design Lineage Solar Panel
Grand Design is recalling 2025–2026 Lineage RVs; solar panels may detach due to adhesive failure.
NHTSA•MODERATENova Bus LFS Transit Bus Control UnitNova Bus is recalling 2022–2023 LFS transit buses; telemetry control unit may shut down and cause loss of drive power.
FDA•MODERATEOphthavet Ophthalmic SolutionDechra is recalling Ophthavet Ophthalmic Solution for dogs and cats due to a lack of sterility assurance.
FDA•MODERATEAtomoxetine HCl 10mg CapsulesSafecor is recalling Atomoxetine HCl 10mg Capsules (NDC 64380-474-01) because some cartons may contain 25mg capsules due to a labeling error.
FDA•MODERATEPhilips Azurion and Allura Imaging SystemsPhilips is recalling Azurion and Allura imaging systems due to hard disk drive failure that may cause loss of functionality or data.
2 products
FDA•CRITICALMalazi 100% Pure Sudanese Sesame TahinaNassar Investment Company is recalling Malazi 100% Pure Sudanese Sesame Tahina due to potential Salmonella contamination.
FDA•MODERATEHiResolution Bionic Ear SystemAdvanced Bionics is recalling the HiRes Ultra 3D CI HiFocus Mid Scala cochlear implant due to an incorrect shelf-life expiration date.
FDA•MODERATEBD Pyxis MedStation 4000 Fingerprint ScannerCareFusion 303 is recalling the BD Pyxis MedStation 4000 medication cabinet due to a fingerprint scanner overheating burn risk.
8 products
NHTSA•MODERATENewmar Freedom Aire Front Chin SpoilerNewmar is recalling 2026 Freedom Aire motorhomes; front chin spoiler may detach during transit.
NHTSA•MODERATEDorman Transmission Gearshift CableDorman is recalling Transmission Gearshift Cables (part numbers 905-146, 905-644, 905-142, BK905-1146-1, BK905-1142-1) due to detachable bushing risking vehicle rollaway.
- NHTSA•MODERATENewmar 2026 Freedom Aire Motorhome Cargo Capacity Label
Newmar 2026 Freedom Aire motorhomes may have incorrect Cargo Carrying Capacity labels, risking overload and crash.
NHTSA•MODERATERoadtrek Recreational Vehicle Pop-Top LatchRoadtrek is recalling 2024–2026 Westfalia Wave SL, Zion Slumber, and other RV models due to pop-top latch disengagement risk during transit.
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta Pharma is recalling Duloxetine Delayed-Release Capsules 30 mg due to the presence of an impurity exceeding FDA recommended limits.
3 products
NHTSA•MODERATEStoryteller Overland 2023 Coolant LinesStoryteller Overland recalls 2023 Stealth, Classic, and Beast Mode AWD vehicles for improperly routed coolant lines causing engine overheating.
FDA•MODERATEErythromycin 250 mg TabletsZydus is recalling Erythromycin 250 mg tablets due to CGMP deviations and the presence of an impurity above acceptable intake limits.
2 products
NHTSA•MODERATEJayco Granite Ridge and Entegra Condor Water Heater Mixing ValveJayco is recalling 2026 Granite Ridge and Entegra Condor motorhomes due to missing water heater mixing valve that could cause scalding.
NHTSA•MODERATEFord Ranger and Bronco Front Seat FrameFord is recalling 2024–2026 Ranger and Bronco vehicles over loose front seat frame bolts that may fail to restrain occupants in a crash.
NHTSA•MODERATELode-King Trailer Rear Impact GuardLode-King is recalling 2019–2026 SDG53-3, SDF53-3, and SDF50-3 trailers with defective rear impact guards that may not protect following vehicles in a crash.
NHTSA•MODERATEHarley-Davidson Motorcycle Airbox BaseplateHarley-Davidson is recalling 2024–2026 FLTRX, FLHX, FXBR, FLFB and other models with Airbox Baseplate 29000373 due to risk of pressurized oil ejection.
FDA•CRITICALLactated Ringer's Injection USPB. Braun Medical is recalling Lactated Ringer's Injection USP due to the presence of particulate matter.
FDA•MODERATEProspector Popcorn Belgian Chocolate ToffeeProspector Popcorn Belgian Chocolate Toffee (UPC 850073852125) recalled for undeclared soy lecithin.
2 products
FDA•CRITICALMA Cohen's Kippered HerringShining Sea Fish Co. is recalling MA Cohen's Kippered Herring due to potential Clostridium botulinum contamination.