FDA•MODERATE
Sea Moss Gel Superfood
Diva Fam is recalling Sea Moss Gel Superfood due to potential Clostridium botulinum contamination.
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FDA•MODERATEAPTUS 2.5 TriLock Screw 16mmMedartis is recalling APTUS 2.5 TriLock Screw 16mm (Model A-5750.16/1) due to a packaging mix-up with 2.8mm screws.
2 products
FDA•MODERATEMaquet Venous Bubble SensorMaquet is recalling Venous Bubble Sensors for 3/8" x 3/32" tubing due to cable durability issues that may cause sensor failure.
NHTSA•MODERATE2026 Range Rover Sport Certification LabelLand Rover is recalling 2026 Range Rover Sport vehicles with incorrect weight information on the certification label, increasing crash risk.
NHTSA•MODERATECooper Discoverer SRX TiresGoodyear is recalling Cooper Discoverer SRX 255/50R20 tires with incorrect Tire Identification Numbers.
FDA•MODERATEFDR Visionary Suite X-ray GeneratorFDR Visionary Suite X-ray generators are being recalled due to a risk of overheating and smoke caused by faulty electromagnetic contactors.
FDA•MODERATEDiowave 250W Laser SystemDiowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.
FDA•MODERATESmoked Grouper DipIsland Crab Corporation is recalling Smoked Grouper Dip due to undeclared milk, eggs, and sodium metabisulfite.
FDA•MODERATEMedline Kits with Tego ConnectorsMedline is recalling kits with Tego Connectors due to seal defects that may cause fluid leakage, therapy delays, or contamination risks.
6 products
FDA•MODERATEOlympus ShockPulse-SE Lithotripsy System GeneratorOlympus is recalling ShockPulse-SE Lithotripsy System generators due to a mis-wired component that may cause treatment delays.
2 products
FDA•MODERATEGluten Free Seasoned Vegan Pizza CrustRich Products Corp is recalling Gluten Free 14" Seasoned Vegan Pizza Crust due to undeclared milk and egg allergens.
2 products
FDA•MODERATEHannaford Hamburger Dill Pickle ChipsHannaford hamburger dill pickle chips (UPC 0 41268 14889 9) recalled due to glass contamination.
FDA•MODERATEOlympus Single Use 3-Lumen Sphincterotome VOlympus is recalling the Single Use 3-Lumen Sphincterotome V due to a manufacturing defect that may cause the device to deform and lose function.
30 products
FDA•MODERATEMedline Convenience KitsMedline is recalling various surgical and biopsy convenience kits due to potential issues with sterilization and packaging equipment calibration.
62 products
FDA•MODERATEPhilips Brilliance iCT Gantry Rotor FastenersPhilips is recalling Brilliance iCT CT systems because loose gantry rotor fasteners could cause parts to become unsecured or expelled.
4 products
NHTSA•MODERATEAptany Eco Sendero M/T2 TireWanli is recalling Aptany Eco Sendero M/T2 tires (LT265/75R16) due to sidewall separation risk.
- Device RecallFDA•MODERATEMint Lesion Software
Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient linking.
FDA•MODERATEMedline Convenience KitsMedline is recalling convenience kits due to potential issues with the sterilization process that may affect product sterility.
58 products
FDA•MODERATEKarison PanjiriKarison is recalling Panjiri due to an undeclared milk allergen.
5 products
FDA•MODERATEPrismaflex M100 SetVantive is recalling the Prismaflex M100 Set due to a potential dislodgement of the deaeration chamber from the control unit.
8 products
FDA•LOWStraumann WB Impression Post Closed TrayStraumann is recalling WB Impression Post Closed Tray kits (L 13mm) due to incorrect magenta impression caps instead of brown.
NHTSA•MODERATEBlue Bird Vision and All American Bus Wheelchair RestraintBlue Bird is recalling 2026 Vision and All American buses with QRT-Deluxe and QRT-Max wheelchair restraints that may not lock.
FDA•MODERATEAQ 120 GFEW Aquarion Preserved CartridgesEncon Safety Products is recalling AQ 120 GFEW Aquarion Preserved Cartridges due to cGMP manufacturing deviations.
FDA•MODERATEVITEK 2 Gram-negative Susceptibility CardsBioMérieux is recalling 30+ VITEK 2 susceptibility card variants over risks of quality control failures and false resistant test results.
2 products
FDA•MODERATERaz Mobile Shower Commode ChairsRaz Design is recalling various mobile shower commode chairs due to a seat bracket installation issue that may cause seat instability.
2 products
FDA•MODERATEMedline Nail KitMedline is recalling the Nail Kit (model DYKM1528) due to potential sterility issues with the included saline wound wash.
5 products
FDA•MODERATEEMPOWR Acetabular System and Knee Tibial InsertsEncore Medical is recalling EMPOWR acetabular system liners and knee tibial inserts due to a packaging discrepancy that may delay surgery.
2 products
NHTSA•MODERATELS2 Rebellion Motorcycle HelmetLS2 Rebellion helmets (XL, XXL, July 2024–July 2025) recalled for inadequate impact protection.
NHTSA•MODERATERivian R1S and R1T Toe Link JointRivian is recalling 2022–2025 R1S and R1T vehicles; toe link joint may separate after service, increasing crash risk.
NHTSA•MODERATEBlue Bird All American Transit Bus 12-Volt CableBlue Bird is recalling 2022–2024 All American transit buses over a loose 12-volt cable that may cause loss of brake assist, drive power, and steering.
FDA•MODERATEHalyard Transport Bag Kit LIFE0080-01Halyard Transport Bag Kit LIFE0080-01 recalled due to Tyvek bag seal issue that may compromise sterility.
FDA•MODERATEATEC Lateral Navigation Disc Prep InstrumentsAlphatec Spine is recalling ATEC Lateral Navigation Disc Prep Instruments due to a design issue with the navigated array connection geometry.
2 products
FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla is recalling Lanreotide Injection 120 mg/0.5 mL (NDC 69097-870-67) due to particulate matter contamination.