FDA•MODERATE
Ortho Dev. Trimax Lantern Knee Drill Plate
Ortho Dev. Trimax Drill Plates for the Lantern Knee System are recalled due to a manufacturing error causing excessive bone cut depth.
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FDA•MODERATEArtegraft Vascular GraftLeMaitre Vascular is recalling the Artegraft Vascular Graft due to a labeling mix-up on the outer packaging.
FDA•MODERATEPuracol and Puracol Plus Collagen Wound DressingsMedline is recalling Puracol collagen wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.
FDA•MODERATEEndoVive Safety PEG KitBoston Scientific is recalling EndoVive Safety PEG Kits due to potentially compromised sterile packaging on the included ChloraPrep swabsticks.
CPSC•Aroeve Air Purifier Model MK04Aroeve air purifier model MK04 (serial "BN") recalled for fire and burn hazard due to overheating.
FDA•MODERATEFrozen Cooked Medium ShrimpH & N Group is recalling 1 lb bags of frozen cooked medium shrimp due to potential Cesium-137 contamination.
FDA•MODERATEHortex Spring Vegetable MixHortex Spring vegetable mix is being recalled due to potential glass contamination.
FDA•MODERATECetrorelix Acetate for Injection Kit 0.25 mgMeitheal Pharmaceuticals recalls Cetrorelix Acetate injection kits (NDC 71288-558-90) due to missing or duplicated needles.
FDA•MODERATERefleXion X1 Radiotherapy System Model RXM1000RefleXion X1 Radiotherapy System Model RXM1000 recalled for software defect causing incorrect radiation dose delivery.
FDA•MODERATEID NOW Influenza A & B 2 Test KitAbbott is recalling ID NOW Influenza A & B 2 test kits due to a higher-than-expected rate of invalid test results.
FDA•MODERATEsmart & simple Turmeric PelletsSmartPak Equine is recalling smart & simple Turmeric Pellets due to elevated aflatoxin levels.
FDA•MODERATEValley Springs 100% Natural Bottled WaterValley Springs is recalling 100% Natural Bottled Water in 1 Gal jugs due to insanitary bottling conditions.
4 products
FDA•MODERATEArtelon FlexBand Dynamic MatrixInternational Life Sciences is recalling the Artelon FlexBand Dynamic Matrix due to failure to meet bacterial endotoxin testing requirements.
3 products
FDA•MODERATEBD Kiestra ReadABD Kiestra ReadA modules may experience connectivity issues after a reboot, potentially delaying plate retrieval.
FDA•MODERATEHitachi Proton Beam Therapy SystemHitachi is recalling the Proton Beam Therapy System (PROBEAT-FR) due to a software anomaly that may cause patient positioning discrepancies.
2 products
CPSC•EnHomee 10-Drawer DresserEnHomee 10-Drawer Dresser (Model 55SCWMSCXLBR) poses tip-over and entrapment hazards to children if not wall-anchored; violates STURDY Act.
CPSC•Andy & Evan Children's Pajama SetsAndy & Evan is recalling children's pajama sets (sizes 2T–6X) due to flammability standard violation and serious burn hazard risk.
CPSC•DriBiz Ammo Tabs Desiccant TilesDriBiz is recalling Ammo Tabs desiccant tiles (Model AMT-010) that may fail to prevent moisture damage to firearms and ammunition, increasing malfunction risk.
CPSC•Lancaster Table & Seating Powder-Coated Aluminum Outdoor Chairs and BarstoolsClark Associates is recalling 180 item numbers of Lancaster Table & Seating outdoor chairs and barstools due to legs that can bend or break, posing a fall hazard.
CPSC•Fixwal 7-Drawer DressersFixwal 7-Drawer Dressers (55.1"L × 11.8"W × 31.5"H) sold on Amazon pose tip-over and entrapment hazards without wall anchoring.
CPSC•PurSteam Elite Travel and Mighty Lil SteamersPurSteam is recalling Elite Travel (PS-510) and Mighty Lil (PS-550) steamers with specific date codes due to risk of hot water expulsion and serious burn injury.
CPSC•Dresbe LED Christmas HeadbandsDresbe LED Christmas Headbands (HB-052) recalled; easily accessible button cell batteries pose ingestion hazard to children.
CPSC•Cobelae Busy BookCobelae Busy Book model 2025-Q3-0702 recalled for detachable beads posing choking hazard.
CPSC•Furnulem 5-Drawer DresserFurnulem recalls five-drawer dressers (Model HK-DS-017-CL-5D-1-W) over tip-over and entrapment risk to children.
CPSC•Little Cow Co. Soy Wax Candles in Glass JarsLittle Cow Co. is recalling 9 oz soy wax candles in glass jars due to risk of cracking or breaking during use.
CPSC•GM Gumili Wintergreen Essential Oil BottlesGM Gumili Wintergreen Essential Oil bottles lack required child-resistant packaging, posing poisoning risk to young children.
CPSC•YITA 16-Drawer Dressers (Multiple Brands)YITA is recalling 16-drawer dressers (Dextrus, ModFusion, Uforic, Yintatech, Yitahome) due to tip-over and entrapment hazards; wall anchoring required.
CPSC•Lotus Joy Sweet Birch Essential OilLotus Joy Sweet Birch Essential Oil recalled for lack of child-resistant packaging; methyl salicylate poisoning risk.
CPSC•Shintenchi 6-Drawer DresserShintenchi 6-drawer dresser (model SHX12077-WH) recalled for tip-over and entrapment hazards; requires wall anchoring.
CPSC•Semfri Children's HelmetsSemfri children's helmets (size M) sold at Walmart.com June–Nov 2025 fail safety standards and pose serious head injury risk.
CPSC•Lola + The Boys Youth Hooded Clothing with DrawstringsLola + The Boys is recalling five youth hooded clothing styles with drawstrings due to strangulation hazard in children.
CPSC•Kitosun Submersible LED LightsKitosun Submersible LED Lights recalled for easily accessible lithium coin batteries posing serious ingestion hazard to children.
CPSC•Organic Zing Birch Essential Oil BottlesOrganic Zing Birch Essential Oil bottles lack required child-resistant packaging, posing poisoning risk to children.
FDA•MODERATETippy Toes Apple Pear Banana Baby FoodTippy Toes Apple Pear Banana baby food is being recalled due to potential patulin contamination.
FDA•MODERATEThiamine HCl InjectionFagron Sterile Services is recalling Thiamine HCl 500 mg injection due to a lack of assurance of sterility.
5 products
FDA•MODERATECampy CVA MediumRemel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.
FDA•MODERATESTA Liatest D-Di KitDiagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias in D-Dimer measurements that may cause inaccurate results.
2 products
CPSC•Scepter B62 Fuel ContainersScepter B62 fuel containers lack flame mitigation and child-resistant spouts, posing flash fire and burn risks.
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•MODERATESTA Liatest Free Protein SDiagnostica Stago is recalling STA Liatest Free Protein S kits due to the risk of inaccurate test results for normal patient plasma levels.
FDA•MODERATEReact Health PHOENIX 5L Oxygen ConcentratorReact Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.
FDA•MODERATEIvenix Infusion System Large Volume PumpFresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.
FDA•MODERATEPure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep ResetPure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.
FDA•MODERATECoco's Italian Market Cannoli Making KitCoco's Italian Market is recalling its 8 oz. Cannoli Making Kit due to undeclared wheat and milk allergens.
2 products
FDA•MODERATEEquinoxe Ergo Modular Impactor HandleExactech is recalling the Equinoxe Ergo Modular Impactor Handle due to a missing cross-pin that may cause device failure.
2 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.
FDA•MODERATEIBA Proton Therapy System PROTEUS 235IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.
FDA•MODERATEPro Numb Tattoo Numbing SprayPro Numb is recalling 5% Lidocaine Tattoo Numbing Spray due to cGMP manufacturing deviations.
2 products
FDA•MODERATEB. Braun Winged Infusion SetsB. Braun is recalling 21GA Winged Infusion Sets (Model 7M2802) due to the risk of needle tips being dull, blunt, or breaking during use.
3 products
FDA•MODERATEMICS3 Angled Sagittal Saw AttachmentHowmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment because external screws may loosen and detach during use.