FDA•MODERATE
Welch Allyn Spot Vision Screener VS100
Welch Allyn is recalling the Spot Vision Screener VS100 due to a screen flickering issue that may pose a seizure risk.
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FDA•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.
FDA•MODERATEWawa Reduced Fat Milk 2% 16 ozWawa is recalling 16 oz pints of Reduced Fat Milk 2% due to potential plastic contamination.
4 products
FDA•MODERATEMidodrine Hydrochloride Tablets, USP 5 mgMajor Pharmaceuticals is recalling Midodrine Hydrochloride Tablets 5 mg (NDC 0904-6818-06) due to inadequately sealed blister packaging.
FDA•MODERATESee Luer Cap Set MPC-130Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
FDA•MODERATEMedline Airway Exam Kit Biopsy ValveMedline is recalling Airway Exam Kits containing Olympus biopsy valves due to a risk of rubber fragment detachment during use.
8 products
FDA•MODERATEConvatec EsteemBody Drainable PouchConvaTec is recalling the EsteemBody Drainable Pouch due to a manufacturing issue that may cause the pouch to leak.
3 products
FDA•MODERATEKLG Kesar MukhwasGanesha Enterprises is recalling KLG Kesar Mukhwas (200 gm) for undeclared food colorings and unapproved dye.
FDA•MODERATESemaglutide Compounding APIHarbin Jixianglong Biotech is recalling Semaglutide API due to failures in process and bacterial endotoxin method validation.
2 products
FDA•MODERATEAmantadine HCl Capsules 100 mgAvKARE is recalling Amantadine HCl Capsules 100 mg (NDC 50268-069-15) nationwide due to failed dissolution specifications.
FDA•MODERATEMedtronic MiniMed Infusion PumpsMedtronic is recalling various MiniMed infusion pumps due to potential insulin over- or under-delivery risks.
14 products
FDA•MODERATEMedline ENFit G-Tube Connector KitsMedline is recalling G-Tube care and discharge kits due to connector defects that may cause leakage and fluid loss.
2 products
FDA•MODERATEPurina Nature's Match Sow & Pig Complete FeedPurina is recalling 50 lb bags of Nature's Match Sow & Pig Complete Feed (UPC 804273051451) due to elevated Deoxynivalenol levels.
CPSC•CheerKid Baby Bath SeatsCheerKid baby bath seats (Model BH-222) recalled for tipping risk and drowning hazard.
CPSC•Watkins Highlife Collection Spa Hydromassage Rotary JetsWatkins is recalling Hydromassage rotary jets in Highlife Collection spas (2023–2025) due to entanglement and drowning hazards from suction force.
CPSC•Beloems Adult Portable Bed Rails Model BL-BR201Beloems bed rails (model BL-BR201) recalled for entrapment, asphyxiation, and fall hazards.
CPSC•Fortemotus Direct Adult Portable Bed RailsFortemotus Direct recalls model USFTMTJAS008 adult bed rails (30"×30") sold Aug–Oct 2025 over entrapment, asphyxiation, and fall hazards.
CPSC•SOOWERY 6-Drawer DresserSOOWERY 6-Drawer Dressers (47.2" × 11.8" × 33.3") sold on Amazon pose tip-over and entrapment hazards without wall anchoring.
CPSC•Cositas Colombianas Magnetic Board GamesCositas Colombianas magnetic board games recalled due to loose magnets posing serious ingestion hazard to children.
CPSC•LShome Photoelectric Smoke Detector Fire AlarmsLShome smoke detector alarms (Model XG-7D04-KZ9Z) may fail to sound during fire due to sensing threshold defect.
FDA•LOWEptifibatide Injection 75 mg/100 mLSlate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.
FDA•MODERATEOlympus Endoscope Suction ValvesOlympus is recalling MAJ-1443 and MAJ-1444 endoscope suction valves due to compatibility issues with specific automated reprocessors.
4 products
FDA•MODERATEXZL Jelly SnacksXZL Jelly Snacks are recalled due to undeclared FD&C Yellow #5, Yellow #6, and Red #40 food dyes.
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical is recalling Wrap Aprons due to potential attenuation degradation that may reduce their protective lifespan.
13 products
FDA•MODERATEEmbrace Shoulder Instrument Drill TowerWaldemar Link is recalling the Embrace Shoulder Instrument Drill Tower (645-081/62) due to incorrect article numbers in the surgical manual.
2 products
FDA•MODERATEBD Alaris System with Guardrails Suite MXBD Alaris System labeling lacks required TLS version specification for secure Wi-Fi communication with Point-of-Care Units.
FDA•MODERATEWellsley Farms Farm-Raised Atlantic SalmonWellsley Farms Farm-Raised Atlantic Salmon (32 oz) recalled for Listeria monocytogenes contamination.
FDA•MODERATEVergani 1944 Milano Pandoro Classico Gluten FreeItalianway Import is recalling Vergani 1944 Milano Pandoro Classico Gluten Free due to potential Teflon fragment contamination.
FDA•MODERATEAdbry (tralokinumab-ldrm) Injection 300 mg/2mLLEO Pharma is recalling Adbry injection autoinjectors (NDC 50222-350-91, 50222-350-02) due to wool fiber contamination affecting sterility.
FDA•MODERATEOrtho Dev. Trimax Lantern Knee Drill PlateOrtho Dev. Trimax Drill Plates for the Lantern Knee System are recalled due to a manufacturing error causing excessive bone cut depth.
2 products
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.
- Device RecallFDA•LOWDatascope Cardiosave Battery Charging Station
Datascope is recalling the Cardiosave Battery Charging Station due to a design defect in the left bay that prevents proper battery charging.
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.