FDA•MODERATE
Aquacel Ag Surgical SP Dressing
ConvaTec is recalling Aquacel Ag Surgical SP dressings because they were manufactured with a thickness exceeding specifications.
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FDA•MODERATEWise Onion RingsWise Foods is recalling 3.75 oz bags of Onion Rings due to undeclared colors and the presence of an unapproved color additive.
FDA•MODERATEOlympus Single Use Distal CoverOlympus is replacing the previous design of the MAJ-2315 Single Use Distal Cover used with the EVIS EXERA III Duodenovideoscope.
FDA•Ola-Ola Pounded YamOla-Ola Pounded Yam is recalled due to undeclared milk, which poses a risk to consumers with milk allergies.
- FDA•Ola-Ola Pounded Yam
Ola-Ola Pounded Yam recalled for undeclared milk allergen.
FDA•CRITICALAdams Extract & Spice: 5 productsAdams Extract & Spice recalls 5 seasoning and mix products over undeclared sesame allergen.
5 products
FDA•CRITICALOrganic Whole BlueberriesFrutas y Hortalizas del Sur S.A. is recalling 10 oz bags of Organic Whole Blueberries due to potential E. coli O145:H28 contamination.
FDA•MODERATEPedigree High Protein Chopped Ground DinnerMars Petcare is recalling Pedigree High Protein Chopped Ground Dinner over potential contamination with plastic and metal foreign material.
FDA•CRITICALFusia Asian Inspirations Kimchi & Tofu KimbapFusia Kimchi & Tofu Kimbap recalled due to undeclared fish allergen.
CPSC•AMASKY Nursing PillowsAMASKY nursing pillows are recalled due to a suffocation hazard, as they violate federal safety standards for infant support cushions.
CPSC•Cuisinart Metal Wire Grill BrushesConair is recalling 10+ models of Cuisinart grill brushes because detached metal bristles pose an ingestion and internal injury hazard.
CPSC•Metalux Optimized High Bay LED Light FixturesCooper Lighting is recalling Metalux Optimized High Bay LED light fixtures due to a fire hazard from potential overheating.
CPSC•CVS Health Medicated Hemorrhoidal WipesCVS Health Medicated Hemorrhoidal Wipes are recalled due to non-child-resistant packaging, posing a risk of poisoning to young children.
CPSC•Junpower CR2032 Lithium Coin BatteriesJunpower CR2032 lithium coin batteries are recalled for lacking child-resistant packaging, posing a severe ingestion and chemical burn hazard.
CPSC•POPOOO Jungle Safari LED Finger LightsPOPOOO LED finger lights are recalled due to a risk of serious injury or death from button cell battery ingestion.
CPSC•Rowenta Cordless Vacuum Cleaner BatteriesRowenta is recalling cordless vacuum batteries that can overheat and ignite, posing fire and burn hazards.
CPSC•Gigglescape Under the Sea Popping ToyGigglescape Under the Sea Popping Toys are recalled due to a choking hazard caused by a detachable plastic dome.
CPSC•Topyond Pool Drain Ports with CoversTopyond pool drain ports are recalled due to entrapment and drowning hazards, as they violate federal pool safety standards.
CPSC•Vevor Baby LoungersVevor is recalling baby loungers due to fall and entrapment hazards that violate federal safety standards for infant sleep products.
CPSC•Roman Candles 8 Shot FireworksWinco Fireworks is recalling Roman Candles 8 Shot fireworks (Model RCLR-W8012) due to explosion and burn hazards from tube malfunctions.
CPSC•Unity 7 Shot Aerial Cake FireworksWinco Fireworks is recalling Unity 7 Shot aerial fireworks (model MEF6096) due to tip-over, explosion, and burn hazards.
FDA•MODERATECinacalcet Hydrochloride Tablets 30 mgCipla recalls Cinacalcet HCl 30 mg tablets over N-nitroso impurity above safe limit.
3 products
FDA•MODERATEDextroamphetamine/Amphetamine Extended-Release CapsulesLannett is recalling 5 mg Dextroamphetamine/Amphetamine ER capsules due to a labeling mix-up where capsules contain immediate-release pellets.
FDA•MODERATEAsclemed: Multiple Lidocaine Hcl Injection ProductsAsclemed recalls Accucaine kits and Lidocaine HCl injection ampules over sterility concerns.
2 products
FDA•MODERATEA.T.S. 4000 TS Tourniquet Dual HoseZimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hoses over sterility breach risk.
2 products
FDA•MODERATEGore TAG Thoracic Branch Endoprosthesis Side Branch ComponentGore is recalling 30+ models of the TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation.
2 products
FDA•CRITICALReprocessed Electrophysiology and Ultrasound CathetersMedline is recalling reprocessed catheters due to residual particulate matter that may cause infection or embolism.
FDA•MODERATEBard Acute Drainage TraysBard recalls Acute Drainage trays due to deficient lidocaine ampoules from supplier.
20 products
FDA•MODERATEMedline Gravity SetMedline is recalling gravity sets labeled "Not for Human Use" that were inadvertently shipped to the U.S. market.
FDA•CRITICALMedtronic Harmony Delivery Catheter SystemMedtronic is recalling the Harmony Delivery Catheter System due to a manufacturing defect that may cause the distal tip to detach during use.
FDA•MODERATESolar GI System Water PerfusionLaborie is recalling Solar GI System configurations due to moisture accumulation that may affect pressure measurement performance.
FDA•MODERATECovidien Shiley Disposable Decannulation PlugCovidien is recalling 12+ models of Shiley Disposable Decannulation Plugs due to incorrect labeling regarding DEHP content.
2 products
FDA•Eunha Fisheries Sliced Korean Halibut and Flounder SashimiEunha Fisheries recalls frozen halibut and flounder sashimi due to undeclared wheat, soy, and sesame allergens.
FDA•MODERATEGlucagon Emergency KitLupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.
3 products
FDA•MODERATEProvision Health: 2 productsPH Labs recalls Ocular Plus and Vista MAX supplements for undeclared Yellow #5 allergen.
2 products
FDA•MODERATEGemcitabine InjectionHikma is recalling Gemcitabine Injection due to improper temperature storage.
FDA•MODERATEZeiss Intrabeam Spherical ApplicatorZeiss is recalling the 1.5 cm Intrabeam Spherical Applicator (REF 304534-6000-557) due to failure to meet manufacturing specifications.
FDA•MODERATESiemens ARTIS icono Ceiling SuspensionSiemens is recalling the ARTIS icono ceiling suspension (Model 11328100) because monitor attachment screws may loosen over time.
FDA•CRITICALDSAEK Pack-RX Surgical Convenience KitWindstone Medical recalls DSAEK Pack-RX kits due to contaminated alcohol prep pads.
4 products- Device RecallFDA•MODERATERayCare 2024A SP1 Oncology Information Systems
RaySearch recalls RayCare 2024A SP1 over beam set delivery note data loss risk.
2 products 
FDA•CRITICALHillrom VOLARA System P.CIRCUIT KITBaxter recalls Hillrom VOLARA P.CIRCUIT KIT (REF M08085) over nebulizer cup leakage that may cause oxygen drop and ineffective treatment.
4 products- Device RecallFDA•MODERATEMedela ENFit Enteral Extension Set
Medela is recalling ENFit Enteral Extension Sets due to incorrect connectors that may cause delivery delays or misconnections.
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Xchange Robotic Collimator Changer for the Cyberknife system due to a risk of the collimator falling from its housing.
FDA•MODERATEARTIS icono biplaneSiemens recalls ARTIS icono biplane over potential loss of detector lift movement.
3 products
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Cyberknife Xchange Robotic Collimator Changer due to a risk of the component falling from its housing.
FDA•MODERATECRE Pro Wireguided Dilatation BalloonBoston Scientific recalls CRE Pro Wireguided Dilatation Balloons over potential sterile pouch breach.
12 products
FDA•MODERATEIntelliCuff Portable Cuff Pressure ControllerThe IntelliCuff pressure controller may fail to maintain cuff pressure due to a system leakage error, causing the motor to run continuously.
FDA•MODERATEPilling Wecksorb NeurospongesTeleflex is recalling Pilling Wecksorb Neurosponges and Neurosponge Strips due to potential out-of-specification levels of endotoxins.
2 products
FDA•MODERATEBaxter Adapter for Head PositioningBaxter is recalling the Adapter for Head Positioning due to a risk of the accessory becoming loose and moving during patient positioning.
FDA•CRITICALSpring & Mulberry Date-Sweetened ChocolateSpring & Mulberry is recalling Mango Chili and Pecan Date-Sweetened Chocolate bars due to potential Salmonella contamination.
11 products