FDA•MODERATE
Olympus Endoscope Air/Water and Suction Valves
Olympus recalls endoscope valves MAJ-1444 and MAJ-1443 over reprocessor incompatibility.
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FDA•MODERATEImactis CT-Navigation SystemGE Medical Systems is recalling Imactis CT-Navigation System (Models E85101LA, E85101LP) due to potential needle trajectory/tip position discordance.
CPSC•Frigidaire Gas RangesThe full list of affected model numbers and serial ranges is available on the CPSC recall page.
CPSC•Amazon Basics Camping Folding Pocket KnivesAmazon is recalling Basics Camping Folding Pocket Knives due to a laceration hazard caused by a faulty blade folding mechanism.
CPSC•Tainoki Office ChairsTainoki is recalling Noah, Owen, and Warren office chairs because the base can bend, posing a fall hazard.
CPSC•Goregent Infant WalkersGoregent infant walkers are recalled for failing to meet federal safety standards, posing a serious fall and injury hazard to infants.
CPSC•Aisstxoer Adult Bicycle HelmetsAisstxoer adult bike helmets (model GH018L) are recalled for failing federal safety standards, posing a serious head injury risk.
CPSC•Specialized Turbo Como SL Electric Bicycle ForksSpecialized is recalling all Turbo Como SL electric bicycle forks due to a fatigue crack that poses a fall hazard.
CPSC•Wagner 900 Series Power SteamersWagner is recalling 900 Series power steamers (models 905e, 915e, and 925e) due to a burn hazard from hot water expulsion.
CPSC•BUILT LUUM Light Up TumblersLifetime Brands is recalling BUILT LUUM light up tumblers due to choking and battery ingestion hazards.
FDA•MODERATEDexamethasone Sodium Phosphate Injection, USP 100 mg/10 mLSomerset Therapeutics is recalling Dexamethasone Sodium Phosphate Injection (NDC 70069-025-10/01) due to out-of-specification impurities at expiry.
FDA•MODERATELeksell Gamma Knife Radiosurgery SystemElekta is recalling Leksell Gamma Knife Perfexion, Icon, and Esprit systems due to potential adapter misalignment during radiation delivery.
FDA•MODERATEArtegraft Vascular GraftLeMaitre Vascular is recalling the Artegraft Vascular Graft due to a labeling mix-up on the outer packaging.
FDA•MODERATEConvatec EsteemBody Drainable PouchConvaTec recalls EsteemBody drainable pouches over possible leakage from a manufacturing issue.
3 products
FDA•MODERATEAptima HPV AssayHologic is recalling the Aptima HPV Assay due to the potential for the test to generate invalid or false negative results.
FDA•MODERATECub Pediatric Crib Model FL19HStryker is recalling Cub Pediatric Crib Model FL19H over missing access door warning labels.
FDA•MODERATESTA Liatest D-Di Assay KitDiagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias in D-Dimer measurements that may cause inaccurate test results.
2 products
FDA•MODERATEWillamette Valley Pie: 4 productsWillamette Valley recalls frozen raw Blueberry Crumble Pies (8" & 9") over possible Listeria contamination.
4 products
FDA•MODERATEBlueFrog Foods: 2 For Green Way Farms Of Georgia GasGreenway Farms recalls Garlic and Jalapeno Dill Pickle Chips (16 fl oz) over lack of process authority.
2 products
FDA•MODERATECNC Noodle: 4 Carbonate And Benzoate Of Soda Added AsCNC Noodle recalls Steam Noodles and Zhong Hua Chao Mian Noodles due to undeclared wheat.
4 products
FDA•MODERATEHortex Spring Vegetable MixHortex Spring vegetable mix is being recalled due to potential contamination with glass.
FDA•MODERATETETAS Mireya Cherry Milkshake PopsicleTETAS Mireya Cherry Milkshake popsicles recalled for undeclared soy lecithin allergen.
FDA•MODERATEIcosapent Ethyl CapsulesZydus Pharmaceuticals is recalling Icosapent Ethyl Capsules due to oxidation, which can cause capsule melting and discoloration.
FDA•MODERATEWelch Allyn Spot Vision Screener VS100Welch Allyn is recalling the Spot Vision Screener VS100 (software v3.2.0.1) due to a screen flickering issue that may trigger seizures.
FDA•MODERATEBioCox 60 Type A Medicated ArticleHuvepharma is recalling BioCox 60 Type A Medicated Article due to failure to meet stability specification requirements.
FSIS•MODERATETurkey Stuffed PastriesShaw Bakers alerts on frozen turkey stuffed pastries mislabeled; some contain ham and cheese instead.
FDA•MODERATESimply Nature Spinach BitesDr. Praeger's is recalling Simply Nature Spinach Bites (12 oz) due to possible rodent hair contamination.
FDA•MODERATEChildren's Ibuprofen Oral Suspension 100 mg/5mLTaro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.
- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE recalls Centricity Universal Viewer software over credential exposure risk.
4 products 
CPSC•Playground Swing Set SeatsPlayground swing seats (model 999604) are being recalled due to a fall hazard caused by potential rivet failure.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid results.
CPSC•17 Stories 14-Drawer Dressers17 Stories 14-Drawer dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.
CPSC•ProRider Bicycle HelmetsProRider is recalling various bicycle helmets that fail federal safety standards, posing a serious risk of head injury or death in a crash.
CPSC•LIVEHOM 11-Drawer DressersLIVEHOM 11-Drawer Dressers are recalled due to tip-over and entrapment hazards that pose a risk of serious injury or death to children.
CPSC•Kluster Magnet Chess GamesStoney Games is recalling Kluster magnet chess games due to a serious magnet ingestion hazard that can cause severe internal injury or death.
FDA•MODERATEMedline Cardiac Procedure KitsMedline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.
FDA•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.
3 products
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
FDA•MODERATECocos Wholesale and Imports: 2 productsCoco's Italian Market recalls Cannoli Making Kit and Fettuccini Alfredo for undeclared wheat and milk allergens.
2 products
FDA•MODERATETemozolomide Capsules 5mgRising Pharmaceuticals is recalling Temozolomide Capsules 5mg (NDC 16571-816-51) due to failed impurities and degradation specifications.
FDA•MODERATESemaglutide Injection 2 mg Multi-Dose VialsNew Life Pharma recalls semaglutide 2 mg vials over sterility concerns.
4 products
FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
FDA•MODERATESodium Iodide (I-131) Therapeutic Oral SolutionRadnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.
FDA•MODERATEArtelon FlexBand Dynamic MatrixArtelon FlexBand Dynamic Matrix recalled over failed endotoxin testing.
3 products
FDA•MODERATEBeckman Coulter DxC 700 AU Chemistry AnalyzerBeckman Coulter recalls DxC 700 AU and AU5800 analyzers over software delay risk.
2 products- Device RecallFDA•MODERATEHealthCast Vital Sync Remote Patient Monitoring System
HealthCast is recalling Vital Sync software due to a failure to transmit or receive critical patient bedside monitor alarms.
2 products 
FDA•MODERATEEndoVive Safety PEG KitBoston Scientific is recalling EndoVive Safety PEG Kits due to compromised seals on the included antiseptic swabsticks.
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsUncle Ray's recalls Lowes Foods sour cream & onion chips (8 oz) over inaccurate nutrition and undeclared MSG.
FDA•MODERATEEndo-Model Replacement PlateauEndo-Model Replacement Plateau is recalled due to a risk of bushing detachment from the screw shaft caused by longitudinal fractures.
13 products
FDA•MODERATEGEM Premier 5000 PAKInstrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to errors that may cause ejection and delay patient results.
20 products