FDA•MODERATE
Dentsply Sirona Capsule Mixer
Dentsply Sirona Capsule Mixer recalled over electrical discharge risk when unplugged.
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FDA•MODERATEIntersurgical One-Piece Guedel AirwayIntersurgical recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue, due to potential occlusion.
2 products- Device RecallFDA•MODERATEHamilton Microlab STAR PCT Software
Foundation Medicine recalls Hamilton Microlab STAR PCT v2.0.0 over spontaneous software closures.
FDA•MODERATEEndoFLIP 1 SystemCovidien recalls EndoFLIP 1 System due to 24-hour limit flagging products as expired.
2 products
FDA•MODERATEGrand Central Potato Sourdough BreadGrand Central Bakery recalls Potato Sourdough Breads due to possible metal pieces.
2 products
FDA•MODERATEShoolin Pharma Chem: multiple drugsShoolin Pharma Chem recalls Sildenafil and Tadalafil APIs due to CGMP deviations.
5 products
FDA•MODERATEClear Eyes Maximum Itchy Eye ReliefClear Eyes Maximum Itchy Eye Relief recalled over potential sterility issues.
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•MODERATEMarketside Tomato Bisque Soup KitMarketside Tomato Bisque Soup Kit recalled due to possible Listeria contamination.
- 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•MODERATESchwarzkopf Professional Osis Grip MousseHenkel recalls Schwarzkopf Osis Grip Mousse 6.76 oz cans over explosion risk from packaging leak.
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•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.
FDA•MODERATEDiovan (valsartan) 160 mg TabletsNovartis recalls Diovan (valsartan) 160 mg tablets due to failed dissolution specs.
FDA•LOWHoneyville Yellow Color 1 GallonHoneyville Yellow Color 1-gal recalled for undeclared Red #40 allergen.
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•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.
FDA•MODERATEMirabegron Extended-Release Tablets 25 mgZydus recalls Mirabegron ER 25 mg tablets over nitrosamine impurity.
FDA•MODERATEOribe Serene Scalp Densifying ShampooOribe Serene Scalp Densifying Shampoo recalled over microbial contamination.
FDA•LOWKanni Delight Fresh Frozen Vannamei White ShrimpKanni Delight Fresh Frozen Vannamei White Shrimp recalled over nitrofurans detected in the product.
FDA•MODERATENeuroguard IEP Carotid Stent SystemContego Medical recalls Neuroguard IEP carotid stent system over filter opening failure risk.
FDA•MODERATECOAPTIUM ConnectTISSIUM recalls COAPTIUM Connect nerve repair device over unsubstantiated 36-month shelf life.
8 products
FDA•MODERATEBlom-Singer Classic Indwelling Voice ProsthesisBlom-Singer Classic Voice Prosthesis recalled due to incorrect labeling of flange types.
2 products
FDA•MODERATEGEM Premier 7000 with iQM3Instrumentation Laboratory recalls GEM Premier 7000 with iQM3 due to lysing bag solution concentration issue.
2 products
FDA•MODERATEU2 Total Knee System Femoral Offset BushingU2 Total Knee System femoral offset bushing recalled due to incorrect engraved numbering that may cause misorientation.
2 products