FDA•
Khong Guan Glutinous Rice Balls with Black Sesame Filling
Khong Guan expands recall of glutinous rice balls with black sesame filling due to undeclared peanuts.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
FDA•MODERATEBD ChloraPrep Clear ApplicatorsCareFusion is recalling BD ChloraPrep Clear sterile solution applicators due to a potential lack of sterility from incomplete packaging seals.
FDA•MODERATEPhotera 400 Phototherapy DeviceDaavlin recalls Photera 400 phototherapy device due to incorrect UV sensor GAIN causing wrong output.
3 products
FDA•MODERATEMedline Total Knee PackMedline recalls Total Knee Pack kits with Zimmer Biomet bowls and spatulas over sterility risk.
2 products
FDA•MODERATEVasoview Hemopro 2 Endoscopic Vessel Harvesting SystemVasoview Hemopro 2 Endoscopic Vessel Harvesting System is recalled due to an out-of-specification sterilization dose.
FDA•MODERATEMedtronic DLP One-Piece Pediatric Arterial CannulaMedtronic recalls DLP Pediatric Arterial Cannula (CFN 77010) over loose foreign material risk.
2 products
FDA•MODERATEPapablic Replacement Brush HeadsPapablic recalls Replacement Brush Heads model Papablic18B due to breakage risk.
2 products
NHTSA•MODERATEOrange EV Terminal Truck Frame RailsOrange EV is recalling certain e-TRIEVER, T-Series, and HUSK-e terminal trucks due to frame rails that may crack and separate.
- Vehicle RecallNHTSA•MODERATEE-One Emergency Vehicles
E-One is recalling 2025-2026 Commercial, Typhoon N, and Cyclone N emergency vehicles due to a risk of sudden loss of drive power.
NHTSA•MODERATENissan Armada, Infiniti QX56, and QX80 Certification LabelsNissan is recalling certain Armada, QX56, and QX80 vehicles with 22-inch wheels due to incorrect GAWR labels that may lead to overloading.
FDA•MODERATECleviprex Injectable EmulsionChiesi USA is recalling Cleviprex (clevidipine injectable emulsion) 50 mg/100 mL vials due to a lack of assurance of sterility.
FDA•MODERATEAmy's Organic Lentil Soup Light in SodiumAmy's is recalling 14.5 oz cans of Organic Lentil Soup Light in Sodium due to potential spoilage.
FDA•MODERATEOla-Ola Pounded GroundnutsOla-Ola Pounded Groundnuts are recalled due to undeclared peanuts, posing a risk to consumers with peanut allergies.
FDA•MODERATEBell Pharmaceuticals: Multiple Carbamide Peroxide ProductsBell Pharmaceuticals recalls store-brand carbamide peroxide ear drops for subpotency (low pH, ~0.6% assay).
11 products
FDA•MODERATEWY Duck Sauce PacketsW.Y. Industries is recalling 0.35 oz. packets of WY Duck Sauce due to potential metal fragment contamination.
FDA•MODERATEOrthofix MINIRAIL External Fixation DeviceOrthofix recalls MINIRAIL external fixation devices due to incorrect labeling.
8 products
FDA•MODERATERuby Quartered Artichoke HeartsRuby Quartered Artichoke Hearts are being recalled due to potential glass contamination.
FDA•CRITICALD'Dioses Fruit Pops: multiple undeclared allergens32 D'Dioses Fruit Pops products recalled for undeclared tree nuts or milk.
32 products
FDA•MODERATEWinfield's CWB Chocolate BarsWinfield's CWB Chocolate Bars recalled for undeclared milk allergen.
NHTSA•MODERATEWinnebago Navion and View Rooftop Ventilation FanWinnebago is recalling 2027 Navion and View RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board fire risk.
NHTSA•MODERATEHyundai Kona Rear Center Seat Belt BuckleHyundai is recalling 2025 Kona Electric and 2026 Kona vehicles because the rear center seat belt buckle may fail to restrain occupants.
NHTSA•MODERATEFord Explorer Roof Rail CoversFord is recalling 2016-2019 Explorer vehicles because roof rail covers may detach, creating a road hazard.
NHTSA•MODERATEFord Aviator and Explorer Second-Row SeatsFord is recalling 2020-2027 Aviator and 2020-2026 Explorer vehicles because a faulty seat switch may cause second-row seats to move unexpectedly.
- Equipment RecallNHTSA•MODERATEFord F-150 Integrated Trailer Module Accessory Kits
Ford is recalling ITRM accessory kits for 2021-2026 F-150s due to a potential loss of trailer brakes and lighting.
NHTSA•MODERATEWabash Dry Freight Truck Liftgate Deck PinsWabash is recalling 2025-2026 Dry Freight trucks because broken liftgate deck pins may cause the platform to fall, posing an injury risk.
FDA•Khong Guan Glutinous Rice Balls with Black Sesame FillingKhong Guan recalls Glutinous Rice Balls with Black Sesame Filling due to undeclared peanuts.
FDA•MODERATEPillsbury Bread Rolls: Hard Roll Dough and Kaiser Roll DoughGeneral Mills is recalling Pillsbury Hard and Kaiser roll dough products due to potential glass contamination.
2 products
FDA•MODERATENystatin Cream USPPadagis is recalling 15 g tubes of Nystatin Cream USP due to subpotent drug results found during stability testing.
FDA•MODERATEOptima XR200/220/240amx Column Safety PawlGE HealthCare recalls Optima XR200/220/240amx systems over column safety pawl testing issue that could cause arm drop and patient injury.
3 products
FDA•MODERATENutricia North America: 2 productsNutricia recalls Liquid Hope and Nourish organic meal replacements due to subpotent vitamin A.
2 products
CPSC•Cuisinart Propel+ Four Burner 3-in-1 Gas GrillCuisinart is recalling the Propel+ Four Burner 3-in-1 Gas Grill (model CGG-6331) because the pizza oven glass can shatter, posing a laceration risk.
FDA•MODERATEBoston Scientific Rapid Refill Continuous Injection SystemBoston Scientific is recalling the Rapid Refill Continuous Injection System due to a risk of syringe disconnection during use.
FDA•MODERATEICU Medical Plum Duo Infusion PumpICU Medical recalls Plum Duo Infusion Pump v1.2.3 due to risk of delivering up to twice the programmed volume.
2 products
FDA•CRITICALAbiomed Impella Introducer SheathOscor recalls Abiomed Impella introducer sheaths (14Fr, 23Fr) due to leakage risk from sidearm and hub.
3 products
FDA•CRITICALTransvenous Pacing Electrode TrayArgon Medical recalls Transvenous Pacing Electrode Trays over non-sterile lidocaine ampules.
6 products
FDA•CRITICALAbiomed Impella RP Flex Introducer KitAbiomed recalls Impella RP Flex introducer kits over sheath leakage risk from manufacturing defects.
13 products
FDA•MODERATEOlympus Toomey Evacuator 30cc with AdaptorOlympus recalls Toomey Evacuator 30cc with Adaptor, Model 188, over sterilization concerns.
4 products
NHTSA•MODERATENAPA Steering Inner Tie Rod EndsTenneco Automotive is recalling NAPA steering inner tie rod ends distributed nationwide due to a risk of steering loss.
NHTSA•MODERATEGrand Design Lineage MaxxAir Rooftop Ventilation FanGrand Design is recalling 2026-2027 Lineage RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board that poses a fire risk.
- Equipment RecallNHTSA•MODERATEZoox Automated Driving System Software
Zoox is recalling ADS software that may fail to detect heavy smoke, increasing the risk of a crash in low-visibility conditions.
CPSC•Insignia Gas RangesInsignia gas ranges (models NS-RGFGSS1 and NS-RGFCGS2) are recalled due to a fire hazard from knobs that can be accidentally activated.
CPSC•BBRKIN and MouTec Biometric Gun SafesBBRKIN and MouTec biometric gun safes are recalled because the locks can be opened by unauthorized users, posing a serious injury risk.
CPSC•Flaunt MagSafe Battery ChargersFlaunt is recalling MagSafe Battery Charger model E33A due to fire and burn hazards from the lithium-ion battery overheating.
CPSC•Kobalt 24V and 48V Yard Power ToolsGreenworks is recalling 20+ models of Kobalt yard power tools due to a fire hazard when charging batteries via the USB-C port.
CPSC•Moodooy Adult Portable Bed RailsMoodooy model F311 adult portable bed rails are recalled due to serious entrapment and asphyxiation hazards.
CPSC•WonderStone Infant WalkersWonderStone infant walkers are recalled due to a fall hazard; they fail to meet mandatory safety standards for doorway and step-edge stopping.
FDA•MODERATEVersius Surgeon ConsoleCMR Surgical is recalling the Versius Surgeon Console due to a cybersecurity risk involving the Secure Boot feature.
- Device RecallFDA•MODERATETMINI Miniature Robotic System Tracking Arrays
Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays because a loose knob may cause surgical misalignment.
FDA•MODERATEVitek 2 AST-N447 Test KitBiomerieux is recalling Vitek 2 AST-N447 Test Kits due to potential for false resistant results caused by pouch foil fractures.
FDA•MODERATEOmniTract Surgical Retractor SystemIntegra LifeSciences is recalling the OmniTract Surgical Retractor System due to insufficient drying time instructions in the user manual.