FDA•MODERATE
Bakkavor: 3 products
Bakkavor recalls focaccia bread and pizza due to possible metal fragments from roasted tomatoes.
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FDA•MODERATEI.T.S. Headless Compression Screw SystemI.T.S. is recalling Headless Compression Screw System components due to updated MRI safety testing showing higher temperature risks.
24 products
FDA•CRITICALHandy Solutions Neck & Shoulders Heating PadHandy Solutions Neck & Shoulders Heating Pad (Model 25607) may overheat and cause burns if folded or placed under the body.
FSIS•CRITICALCS Beef Packers Ground Beef ProductsCS Beef Packers recalls 22,912 lbs of ground beef (case codes 18601, 19583, 19563) over E. coli O145 contamination; do not serve.
3 products
FDA•MODERATEAjinomoto Foods North America: 11 productsAjinomoto recalls frozen fried rice and gyoza dumplings over possible glass contamination.
11 products
FDA•MODERATEChilli Spanish Peanuts: 2 productsWestern Mixers recalls Chilli Spanish Peanuts (First Street 11 oz, Treasured Harvest 25 lb) due to possible glass contamination.
2 products
FDA•MODERATEKing Harvest Brand: 6 productsKing Harvest hummus recalled due to possible aluminum pieces.
6 products
FDA•MODERATESunflour Bakery Hamburger BunsSunflour Bakery is recalling 18oz hamburger buns due to an undeclared sesame seed allergen.
FDA•LOWSodium Iodide I-131 Kit Gelatin Capsule PackRadnostix is recalling Sodium Iodide I-131 Kit capsule packs due to failed product specifications.
FDA•CRITICALErbe Flexible CryoprobeErbe USA recalls Flexible Cryoprobes because probes may rupture or burst during use.
4 products
FDA•MODERATEOlympus Endoscope Air/Water and Suction ValvesOlympus recalls endoscope valves MAJ-1444 and MAJ-1443 over reprocessor incompatibility.
4 products
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•LOWDatascope Cardiosave Battery Charging StationDatascope is recalling the Cardiosave battery charging station due to a screw defect in the left bay that prevents proper charging.
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•CRITICALHouse of Flavors Chicago Vanilla Ice CreamHouse of Flavors is recalling 3-gallon tubs of Chicago Vanilla Ice Cream due to undeclared egg, posing a risk to those with egg allergies.
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•CRITICALMID EAST Jordanian Zaatar Spice MixKradjian recalls MID EAST Jordanian Zaatar spice mix for undeclared sesame and wheat allergens.
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•CRITICALWebcol Alcohol Prep Pads (70% Isopropyl Alcohol)Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.
3 products
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.
FDA•CRITICALDistribuidora de Alimentos: 2 AzucarsGorditas and Doraditas de Azucar recalled over undeclared Wheat and Soy allergens.
2 products
FDA•CRITICALBluegrass Ingredients: Butter-Rich Powder and Butter PowderBluegrass Ingredients recalls Butter-Rich and Butter Powder (50 lb.) over Salmonella risk.
2 products
FDA•CRITICALMiss Vickies Spicy Dill Pickle ChipsFrito-Lay recalls Miss Vickies Spicy Dill Pickle chips 8 oz bags for undeclared milk allergen.
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.
FDA•LOWPitavastatin Tablets, 2 mgNorthstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.
- Device RecallFDA•MODERATECentricity Universal Viewer Software
GE recalls Centricity Universal Viewer software over credential exposure risk.
4 products 
FDA•CRITICALBlue Bull Extreme Male Enhancement SupplementBlue Bull Extreme Male Enhancement recalled due to undeclared sildenafil.
3 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.