FDA•CRITICAL
Medical Action Industries Pack Cath BHH
Medical Action Industries is recalling Pack Cath BHH kits due to a potential syringe adapter disconnection issue.
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FDA•MODERATEDEX Ophthalmic Tissue ForcepsKatalyst Surgical recalls DEX Ophthalmic Tissue Forceps, model DVF4005-23, due to IFU corrective action.
12 products
NHTSA•MODERATEMicro Bird G5 and MB II School Bus Drive Belt PulleyMicro Bird recalls 2023–2026 G5 and 2024 MB II school buses; drive belt pulley may damage oil lines and cause fire risk.
NHTSA•MODERATEMicro Bird G5 Transit Bus Drive Belt PulleyMicro Bird recalls 2023–2025 G5 transit buses; drive belt pulley may damage oil lines and cause fire risk.
FDA•MODERATEJesse Withrow: 2 Glass Mason Jars With Metal LidsMy Wife's Slaw (original and Jalapeno Heat) recalled for lack of approved food establishment inspection.
2 products
FDA•MODERATEVegan Kale Caesar SaladMarket of Choice recalls Vegan Kale Caesar Salad over undeclared sesame allergen.
FDA•CRITICALMA Cohen's Kippered HerringShining Sea Fish recalls MA Cohen's Kippered Herring due to botulism hazard.
FDA•CRITICALJOHN B SANFILIPPO & SONS: 6 productsJohn B. Sanfilippo recalls nut mixes over Salmonella risk.
6 products
FDA•MODERATEWinfield's Chocolate BarsWinfield's CWB Chocolate Bars recalled over undeclared milk allergen.
FDA•MODERATEAmoxicillin and Clavulanate Potassium Oral Suspension DropsCronus Pharma is recalling Amoxicillin and Clavulanate Potassium oral suspension drops for dogs and cats due to product discoloration.
2 products
FDA•MODERATEWoodstock Organic Shelled EdamameWoodstock Organic Shelled Edamame recalled over possible metal pieces.
FDA•MODERATEOctreotide Acetate for Injectable SuspensionTeva is recalling Octreotide Acetate 30 mg injection kits due to a lack of assurance of sterility.
2 products
FDA•CRITICALCalifornia Dairies: 3 Packed UndersCalifornia Dairies recalls non-fat dried milk and buttermilk powders over possible Salmonella contamination.
3 products
FDA•MODERATEEnalapril Maleate Tablets, USP 20 mgRising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
FDA•MODERATEBD PurPrep Sterile SolutionCareFusion is recalling BD PurPrep sterile solution due to a lack of assurance of sterility and potential product contamination.
2 products
FDA•MODERATEWalker Honey: 10 productsWalker Honey recalls Fain's creamed honey spreads over possible stainless steel and plastic particles.
10 products
FDA•MODERATEHorizon Organic Chocolate Lowfat MilkHorizon Organic recalls Chocolate Lowfat Milk 8-oz boxes due to package integrity issues.
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•MODERATE...And Kimchi Kimchi...And Kimchi kimchi recalled for undeclared fish allergen.
FDA•CRITICALUtz Quality Foods: Zapp's and Dirty Potato ChipsUtz is recalling Zapp's and Dirty potato chips in several varieties for possible Salmonella contamination.
6 products
FSIS•MODERATERavioli Pasta with Beef SauceRana Meal Solutions alerts on ravioli pasta mislabeled as beef and burrata that may contain shrimp and lobster, undeclared allergens.
FDA•MODERATEDELFLEX Peritoneal Dialysis SolutionFresenius recalls DELFLEX dialysis solution due to potential bag leaks compromising sterility.
2 products
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta recalls Duloxetine 30 mg capsules over nitrosamine impurity above FDA limit.
3 products
FDA•CRITICALGriffith Foods: 3 productsGriffith Foods recalls meatloaf seasoning, milk wash, and milk-n-egg mix due to potential Salmonella.
3 products
FDA•MODERATEXZL Jelly SnacksSungal Inc. recalls XZL Jelly Snacks 12.68 oz bags due to undeclared FD&C Yellow #5, #6, and Red #40.
FDA•MODERATEMontebianco Base VeganMontebianco Base Vegan is recalled due to undeclared milk, which exceeds acceptable levels despite the product's warning label.
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators serviced without proper performance inspections, potentially delaying therapy.
NHTSA•MODERATE2026 Toyota 4Runner Load Capacity Label2026 Toyota 4Runner recalled for incorrect load capacity label that may lead to improper loading.
FDA•CRITICALa2 Platinum Premium Infant Formulaa2 Milk recalls a2 Platinum infant formula 31.7 oz over possible Cereulide toxin contamination.
FDA•MODERATESecond Nature Keto Crunch Smart MixSecond Nature recalls Keto Crunch Smart Mix 10 oz pouches due to undeclared cashews, pistachios, and dried cherries.
FDA•MODERATESpacelabs Ultraview SL Command ModuleSpacelabs is recalling the Ultraview SL Command Module due to a manufacturing issue with the electrical leakage tester.
2 products
FDA•MODERATEProdisc C SK Cervical Disc ImplantCentinel Spine recalls Prodisc C SK cervical disc implants due to labeling mix-up (5mm/6mm).
2 products
FDA•CRITICALHalyard Cardiac Cath Pack KitAVID Medical recalls Halyard Cardiac Cath Pack kits over risk of syringe adaptor disconnection.
10 products
FDA•CRITICALCook Centimeter Sizing CatheterCook recalls Centimeter Sizing Catheter (RPN N5.0-35-100-P-10S-PIG-CSC-20) over marker band cracking risk.
3 products
FDA•MODERATEBoston Scientific LUX-DX II Arrhythmia DetectorBoston Scientific recalls LUX-DX II Arrhythmia Detector (M302) with LATITUDE DRAGON US Server (6460) over missing PVC Burden and Bradyarrhythmia monitoring.
2 products
FDA•MODERATEERBEFLO CleverCap CO2 Tubing/Cap SetsErbe Medical recalls ERBEFLO CleverCap CO2 tubing/cap sets due to risk of water aspiration and respiratory failure.
3 products- Device RecallFDA•MODERATEda Vinci Surgical System Universal Surgical Manipulator
Intuitive Surgical is recalling the USM arm sub-assembly for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products 
FDA•CRITICALVOCSN V+Pro Respiratory SystemVentec is recalling VOCSN V+Pro respiratory systems (REF: PRT-01198-000, PRT-01185-000) due to potential oxygen leaks that may increase fire risk.
FDA•CRITICALIntuitive SureForm 30 Gray ReloadsIntuitive is recalling SureForm 30 Gray stapler reloads due to the risk of an incomplete staple line during surgical procedures.
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.
FSIS•MODERATEMeat and Poultry Products with Recalled Dairy IngredientsFSIS alert: meat & poultry products with recalled dairy ingredients may be contaminated with Salmonella.
FDA•MODERATEMy Mochi Strawberry Non-Dairy Frozen DessertMy Mochi Strawberry Non-Dairy Frozen Dessert recalled due to foreign object in container.
FDA•MODERATECalypso Tropic Tango LemonadeCalypso Tropic Tango Lemonade recalled for undeclared Yellow No. 5.
FDA•MODERATEKLG Kesar MukhwasGanesha Enterprises is recalling KLG Kesar Mukhwas (200 gm) for undeclared food colorings and unapproved dye.