FDA•MODERATE
Weis Pasteurized Apple Cider
Weis Markets recalls Fresh From the Orchard pasteurized apple cider over high patulin levels.
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FDA•CRITICALRon's Home Style Foods: 2 productsRon's Home Style Foods recalls 5 lb Pico de Gallo and Salsa Autentica over potential Salmonella contamination.
2 products
FDA•LOWDoxylamine Succinate and Pyridoxine HCl Delayed-Release TabletsBionpharma recalls Doxylamine Succinate and Pyridoxine HCl 10 mg/10 mg tablets over foreign tablets or capsules.
FDA•MODERATESTA Staclot Protein SDiagnostica Stago recalls STA Staclot Protein S reagent over QC drift within its 4-hour stability period.
FDA•MODERATEBaxter Healthcare: multiple drugsBaxter recalls 17 sterile injectable drugs, including Vancomycin and Clindamycin, over CGMP deviations.
17 products
FDA•MODERATEHalyard Medical Convenience KitsAVID Medical recalls 80+ Halyard convenience kit variants over endotoxin variability in Ritmed Neurological Sponges.
3 products
FDA•MODERATEApheresis Platelets, PAS, Leukocytes Reduced, Pathogen ReducedRed Cross recalls Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced, not tested for pH.
NHTSA•MODERATEHeartland Bighorn Certification Label GAWRJayco recalls certain 2027 Heartland Bighorn trailers over an incorrect GAWR on the certification label, risking overload and crash.
NHTSA•MODERATEMagic Tilt Aluminum PWC Boat Trailer WinchMagic Tilt is recalling certain 2025-2026 aluminum PWC boat trailers because the winch weld may fail, causing detachment and injury risk.
FDA•MODERATEPaxil CR Paroxetine 37.5mg TabletsApotex recalls Paxil CR 37.5mg tablets for failing dissolution specs.
FDA•MODERATEMehadrin Chocolate Leben 6 oz CupsMehadrin Chocolate Leben 6 oz cups recalled due to improper pasteurization.
FDA•MODERATEHorizon Organic Chocolate Milk 8 ozHorizon Organic recalls 1% chocolate milk 8 oz Tetra Paks over potential spoilage.
- Device RecallFDA•MODERATEPortrait Core Services Software V1.1
GE Medical recalls Portrait Core Services Software V1.1 over possible loss of patient monitoring and alarm reset issues.
4 products 
NHTSA•MODERATEAltec Service Body Strobe LightAltec recalls 2021-2023 Service Body vehicles: strobe light water leak can short-circuit, fire risk.
FDA•MODERATERamipril Capsules USP 10 mgHikma recalls Ramipril Capsules USP 10 mg over a failed impurity (DCU) specification.
FDA•MODERATEICU Medical IV Sets with Drip ChambersICU Medical recalls IV sets with drip chambers due to black specks that may delay therapy.
FDA•LOWAfricando Alfredo Hot SauceAfricando Alfredo Hot Sauce recalled for undeclared wheat and soy allergens.
FDA•MODERATEByron White Formulas: 3 May Contain Nuts CasByron White Formulas recalls A-L Complex, A-FNG, and A-P herbal supplements due to undeclared walnuts.
3 products
FDA•MODERATEOlympus PowerSeal 5 mm Curved Jaw Sealer & DividerOlympus recalls PowerSeal 5 mm Curved Jaw Sealer & Divider over labeling error.
FDA•MODERATEZicam Medicated Nasal SwabsZicam nasal swabs recalled over microbiological testing failures.
FDA•MODERATEIMRIS ORT200 Operating Room TableIMRIS recalls ORT200 operating room tables due to actuator/lock failure risk of unintended movement.
2 products
FDA•MODERATEActhar Gel (Repository Corticotropin Injection) 5 mL VialsMallinckrodt recalls Acthar Gel 5 mL vials over glass and stopper particulate.
2 products
FDA•MODERATEClobetasol Propionate Cream USP, 0.05%Lupin recalls Clobetasol Propionate Cream 0.05% due to failed content uniformity.
FDA•MODERATEhealthmark ProChek-II TestHealthmark recalls ProChek-II tests (PT-313, PT-201-12) over expired ingredient risk.
2 products- Device RecallFDA•MODERATEFUJIFILM Synapse PACS Software
FUJIFILM Synapse PACS v7.4.310 recalled due to inaccurate ruler measurements.
FDA•MODERATEMedline Femoral Pack and FEVAR KitsMedline recalls Femoral Pack and FEVAR kits due to potentially contaminated component.
14 products
FDA•MODERATEGENESYS CrossFT Suture AnchorConMed recalls GENESYS CrossFT Suture Anchor (REF CFBC-5502B) due to incorrect implant card.
FDA•MODERATEFresenius 2008T BlueStar Hemodialysis MachineFresenius recalls 2008T BlueStar Hemodialysis Machine over flow, no water, and temperature alarms.
NHTSA•CRITICALBell Pit Boss HelmetsBell is recalling certain Pit Boss helmets (size medium, 2025-2026) over inadequate impact protection, violating FMVSS 218.
FDA•CRITICALBaxter Dextrose Injection 70% 2000 mL BagsBaxter recalls Dextrose Injection 70% 2000 mL bags over stainless steel particles.
FDA•CRITICALJalapeno RanchJaime's Foods recalls Jalapeno Ranch 16 oz jars due to undeclared egg allergen.
FDA•LOWIbuprofen Oral Suspension SyringesSafecor recalls Ibuprofen oral suspension syringes over cross-contamination risk.
FDA•MODERATEStructur 2 SC Temporary Resin Cartridge RefillHenry Schein recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm due to incorrect packaging and IFU.
2 products
FDA•MODERATEMidmark IQecg Digital ECGMidmark recalls IQecg Digital ECG over incorrect ECG waveforms and BPM calculations.
2 products
FDA•MODERATECanon Alphenix Ceiling Movement Gear ScrewsCanon recalls Alphenix X-ray systems (INFX-8000C/F/V) over loose ceiling gear screws.
NHTSA•MODERATEMitsubishi Outlander Rearview CameraMitsubishi recalls 2025-2026 Outlander and 2026 PHEV for rearview camera display failure.
NHTSA•MODERATEFord Maverick, F-150, Bronco Sport Vehicle JointsFord recalls certain 2026 Maverick, F-150, and Bronco Sport vehicles over improperly tightened joints that may cause crashes or fires.
NHTSA•MODERATEFord 2026 Explorer, Bronco, Bronco Sport, Mustang, Ranger PistonsFord recalls certain 2026 Explorer, Bronco, Bronco Sport, Mustang, and Ranger vehicles over piston dome failure risk.
- NHTSA•MODERATEFord Mustang Wiring Harness Ground Connection
Ford recalls 2024-2026 Mustangs over wiring harness ground connections that may fracture, causing loss of drive power or visibility.
FDA•CRITICALTyenne (tocilizumab-aazg) Injection 400 mg/20 mLFresenius Kabi recalls Tyenne ( (tocilizumab-aazg) 400 mg/20 mL vials over glass particles.
FDA•MODERATERemedy+ Recovery Dogswell Pet WormerRemedy+ Recovery Dogswell Pet Wormer recalled due to adverse event complaints.
NHTSA•MODERATEThomas Built SAF-T-LINER HDX2 and EFX2 Seat Belt AnchorDaimler Trucks recalls 2027 Thomas Built SAF-T-LINER HDX2/EFX2 buses over missing seat belt anchor connector plates.
NHTSA•MODERATERennline Lower Control ArmRennline is recalling lower control arms (part S180) that may damage the subframe and cause loss of steering control.
FDA•CRITICALFromm Family Foods: 2 Wet Dog Food Packaged In CodesFromm recalls Turkey Pate and Milo's Meatloaf Pate wet dog foods over possible metal contamination.
2 products
FDA•CRITICALSirna & Sons Jalapeño Peppers 1 lbSirna & Sons recalls 1 lb jalapeño peppers over potential Salmonella Javiana.
FDA•MODERATELevothyroxine Sodium Tablets 25 mcgAccord recalls Levothyroxine 25 mcg tablets due to subpotency.
12 products
FDA•MODERATEHalyard Davinci TruCustom Foley TrayHalyard Davinci TruCustom Foley tray recalled over missing latex warning on StatLock component.
8 products
FDA•MODERATEMerge PACS and Merge OrthoPACSMerge PACS and OrthoPACS recalled due to inaccurate measurement display.
FDA•MODERATEAmerican Contract System Convenience KitAmerican Contract Systems recalls Convenience Kit CV B PACK (TNCB10AM) due to catheter performance failure.
4 products- Device RecallFDA•MODERATEPhilips Incisive CT Software
Philips Incisive CT software V4.5/V5.0 recalled for Bolus Tracking scan trigger failure.