FDA•MODERATE
Clear Eyes Maximum Itchy Eye Relief
Clear Eyes Maximum Itchy Eye Relief recalled over potential sterility issues.
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FDA•MODERATERed Blood Cells, Leukocytes ReducedRed blood cell units distributed after donor tested reactive for hepatitis C antibody.
- FDA•MODERATERed Blood Cells, Leukocytes Reduced
Hoxworth recalls Red Blood Cells, Leukocytes Reduced due to malaria risk from donor travel.
FDA•MODERATEPresource KitsCardinal Health is recalling multiple Presource procedural kits due to possible endotoxin contamination.
13 products
FDA•MODERATEBD Intravascular Administration and Extension SetsBD recalls IV administration and extension sets due to possible sterilization failure.
2 products
FDA•CRITICALOma's Pride Woof Complete Canine Chicken RecipeOma's Pride recalls Woof Complete Canine Chicken Recipe frozen dog food over potential Salmonella.
FDA•MODERATEMarketside Tomato Bisque Soup KitMarketside Tomato Bisque Soup Kit recalled due to possible Listeria contamination.
FDA•CRITICALDairyland Jalapeno PeppersDairyland is recalling jalapeno peppers over possible Salmonella contamination.
FDA•CRITICALWhole Foods: Guacamole and Salsa DipsWhole Foods recalls guacamole and salsa dips over possible Salmonella from jalapenos.
10 products- FDA•MODERATEApheresis Red Blood Cells, Leukocytes Reduced
LifeShare Blood Centers recalls apheresis red blood cells, leukocytes reduced, from a donor with incomplete eligibility screening.
FDA•MODERATERed Blood Cells, Leukocytes ReducedLifeShare distributed leukoreduced red blood cells from a malaria-endemic-area donor.
FDA•MODERATEERBECRYO 2 Cryosurgical UnitErbe USA recalls ERBECRYO 2 Cryosurgical Unit (Model 10402-000) over risk of cryoprobe rupture from CO2 leak.
FDA•MODERATEProNephro AKI (NGAL) Reagent KitBioporto recalls ProNephro AKI (NGAL) Reagent Kit over non-validated rework that could cause missed renal disease diagnosis.
FDA•MODERATEBIOFIRE Respiratory Panel 2.1BioFire recalls BIOFIRE Respiratory Panel 2.1 over increased false negatives.
FDA•CRITICALVitasia Asian Style Wok Spice MixVitasia Asian Style Wok Spice Mix recalled due to Salmonella.
FDA•MODERATESchwarzkopf Professional Osis Grip MousseHenkel recalls Schwarzkopf Osis Grip Mousse 6.76 oz cans over explosion risk from packaging leak.
FDA•CRITICALFrankie's Organic Plant-Based Puffs Vegan CheddarFrankie's Organic Plant-Based Puffs Vegan Cheddar recalled over undeclared milk allergen.
FDA•MODERATEStraumann Bone Level Tapered ImplantStraumann recalls BLT Implant D 4.1mm RC SLActive 14mm due to possible 12mm length mismatch.
FDA•MODERATEEndo-Model Tibial Plateau Replacement SetWaldemar Link recalls Endo-Model tibial plateau replacement sets that may contain the wrong hinge component.
FDA•CRITICALBaxter Duo-Vent Solution SetBaxter recalls Duo-Vent Solution Set (1C8507) over air bubble risk in drip chamber and tubing.
FDA•CRITICALMorphine Sulfate Injection 2 mg/mL Prefilled SyringesFresenius Kabi recalls Morphine Sulfate 2 mg/mL syringes over a label mixup that may contain Dilaudid.
2 products
FDA•MODERATEClindamycin Palmitate Hydrochloride Oral SolutionAvet recalls Clindamycin Palmitate Oral Solution 75 mg/5 mL over particles and white flakes.
FDA•MODERATEER-Spec Vaginal SpeculumOBP Medical recalls ER-Spec X-Small vaginal speculums over a sharp-edge burr risk.
- Device RecallFDA•MODERATEPhilips Azurion Interventional X-Ray System
Philips recalls Azurion x-ray systems over software issues that may delay therapy or cause complications.
- Device RecallFDA•MODERATEPhilips Azurion Interventional Fluoroscopic X-Ray System
Philips recalls Azurion X-ray systems over software issues that may cause image degradation or loss of geometry movements.
- FDA•MODERATERed Blood Cells, Leukocytes Reduced
Hoxworth Blood Center recalls Red Blood Cells, Leukocytes Reduced over malaria risk.
FDA•MODERATEGM Helix Dental ImplantStraumann recalls GM Helix dental implants over a packaging label mismatch that could cause bone compression.
FDA•MODERATEPhilips Allura Xper FDPhilips recalls Allura Xper FD x-ray systems over firmware issue causing loss of geometry movements.
FDA•MODERATEGlidesheath Slender A-KitTerumo recalls Glidesheath Slender A-Kit 6F 10cm .021GW (60-1060) due to wrong guidewire.
- Food RecallFSIS•MODERATEJalapeño-Containing Meat and Poultry Products
FSIS alert: meat and poultry products with recalled jalapeños may be contaminated with Salmonella.
FSIS•CRITICALMidamar Beef Pastrami and Corned Beef BrisketCity Foods recalls 3,215 lbs of RTE pastrami and corned beef over Listeria risk; EST. 1896.
3 products
FDA•CRITICALLexunder: 9 Food To LivesLexunder recalls Food to Live organic powdered greens products over possible Salmonella contamination.
9 products
FSIS•CRITICALAl Kabeer Breaded Swai Fish Fillets and SticksShan Distribution recalls 5,084 lbs of Al Kabeer breaded Swai fish fillets and sticks due to import violation.
3 products
FSIS•CRITICALCorte Argentino Raw BeefCorte Argentino recalls 29,628 lbs of raw beef imported without reinspection; affected cuts include Top Sirloin, Eye Round, and more.
5 products
FDA•MODERATEDiovan (valsartan) 160 mg TabletsNovartis recalls Diovan (valsartan) 160 mg tablets due to failed dissolution specs.
FDA•MODERATELyle Style: 2 Made In The Columbia River Gorge WashingtonsUndeclared soy allergen in Lyle Style Bloody Mary Mix.
2 products
FDA•MODERATEVodka Tomato Sauce 24 ozSHEANDRO recalls Vodka Tomato Sauce 24 oz jars for undeclared milk allergen.
FDA•MODERATESemaglutide 12.5mg Multi-Dose VialApollo Care recalls semaglutide 12.5mg vials due to particulate matter.
11 products
FDA•CRITICALGarden Salad 7.75 ozCibus Fresh, Sprig & Sprout, and Jack & Olive Garden Salad 7.75 oz recalled for possible Cyclospora contamination.
FDA•MODERATENeisseria meningitidis Gp C 2ml/VLRemel recalls Neisseria meningitidis Gp C 2ml/VL (R30166901) for failing to test positive within 60 seconds.
FDA•MODERATEMedline Micro-Kill Bleach Germicidal WipesMedline Micro-Kill Bleach Germicidal Wipes may lose disinfecting strength before their 12-month shelf life ends.
4 products
FDA•MODERATEApheresis Platelets, Leukocytes ReducedSuncoast Blood Bank recalls apheresis platelets from a donor with recent malaria-area travel.
FDA•MODERATEV-Loc 90 Absorbable Wuture Closure DeviceCovidien recalls V-Loc 90 wound closure devices over possible sterile barrier tears that may cause infection or prolonged surgery.
7 products
FDA•MODERATEBoston Scientific Enhance Transcarotid/Peripheral Access KitBoston Scientific recalls Enhance Transcarotid/Peripheral Access Kits over detachable depth markings.
FDA•MODERATESpacelabs Xhibit Central Station DisplayPort SplitterSpacelabs recalls Xhibit Central Station over DisplayPort splitter audio/video failures.
2 products
FDA•MODERATEGORE VIABIL Biliary EndoprosthesisGORE VIABIL biliary endoprosthesis recalled due to mislabeling of size and drainage holes.
2 products- Device RecallFDA•MODERATEnavify Digital Pathology Software
Ventana recalls navify Digital Pathology v2.5 over image/metadata discrepancy in the Viewer window.
FDA•MODERATEBOBBY Balloon Guide CatheterMicroVention recalls BOBBY Balloon Guide Catheters due to increased balloon pinhole defects.
CPSC•EEMB Lithium Coin Battery ChargersEEMB recalls Lithium Coin Battery Chargers, model SKLC-0420-0040, due to battery ingestion risk.
CPSC•DR Power PRO MAX30 Walk-Behind Lawn MowersDR Power recalls PRO MAX30 walk-behind mowers over blade control defect posing laceration hazard.