FSIS•CRITICAL
Shera Broadhead Clarias Fish Products
Sobico USA recalls 13,464 lbs of Shera Broadhead Clarias Fish (whole/gutted and steaks) imported without required reinspection; best-before June 23, 2027.
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FDA•MODERATEWillamette Valley Pie Company Blueberry Crumble PieWillamette Valley Pie Company is recalling frozen raw blueberry crumble pies due to potential Listeria monocytogenes contamination.
4 products
FDA•CRITICALMade Fresh Salads Whipped Cream CheeseMade Fresh Salads is recalling 5 lb tubs of Whipped Cream Cheese due to potential Listeria monocytogenes contamination.
14 products
FDA•MODERATETECNIS Eyhance IOL with Simplicity Delivery SystemAMO is recalling TECNIS Eyhance IOLs with Simplicity Delivery Systems because the lens haptic may stick, preventing proper unfolding.
2 products
FDA•MODERATEBioCox 60 Type A Medicated ArticleHuvepharma is recalling BioCox 60 Type A Medicated Article due to failure to meet stability specification requirements.
FDA•CRITICALAll Natural Chicken Chips for DogsElite Treats is recalling All Natural Chicken Chips for Dogs due to potential Salmonella contamination.
FDA•MODERATESunflour Bakery Hamburger BunsSunflour Bakery is recalling 18oz hamburger buns due to undeclared sesame seeds, which pose a risk to those with sesame allergies.
FDA•MODERATEVasocaine SprayHTO Nevada is recalling Vasocaine Spray (Lidocaine HCl 4%, Racepinephrine HCl 0.01%) because stability data does not support the expiry date.
3 products
FDA•MODERATEXTANT MEDICAL Xpress Pedicle Screw SystemXTANT MEDICAL is recalling Xpress Pedicle Screw System 6.5 x 50 mm (X073-6555-DL) due to mislabeling identifying incorrect screw length.
FDA•MODERATEArtoura and CPX 4 Breast Tissue ExpandersMentor Texas is recalling 10+ models of breast tissue expanders due to infusion set needles that may be blunt or break during use.
7 products
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•CRITICALAbiomed Impella Purge CassetteAbiomed is recalling Generation 1 purge cassettes due to an increased risk of purge leaks.
2 products
FDA•MODERATEAptima HPV AssayHologic is recalling the Aptima HPV assay (catalog 303585) due to the potential for invalid or false negative results.
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.
FDA•MODERATECub Pediatric Crib Model FL19HStryker is recalling Cub Pediatric Crib Model FL19H over missing access door warning labels.
FDA•CRITICALBaxter Volara Respiratory Therapy Blue Ventilator Adapter ModuleBaxter is correcting its Volara Respiratory Therapy Blue Ventilator Adapter Module (M07937) due to risks of oxygen desaturation or barotrauma in home care use.
FDA•MODERATEWelch Allyn Spot Vision Screener VS100Welch Allyn is recalling the Spot Vision Screener VS100 due to a screen flickering issue that may pose a seizure risk.
FDA•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.
FDA•CRITICALYoung Again Pet Food Core Health Dog FoodYoung Again Pet Food Core Health Dog Food recalled for presumptive Salmonella; 10 lb and 25 lb bags affected.
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.
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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•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling Automated Impella Controllers due to a potential delay in the "Purge System Blocked" alarm.
2 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•CRITICALRosabella Moringa Dietary Supplement CapsulesAmbrosia Brands is recalling Rosabella Moringa dietary supplement capsules due to potential Salmonella contamination.
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•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical is recalling 20+ models of CentrosFLO Hemodialysis Catheters due to a sheath design defect that may cause serious injury.
5 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.
FDA•CRITICALQuest Cat Food Chicken Freeze Dried NuggetsSteve's Real Food recalling Quest Cat Food Chicken Freeze Dried Nuggets (10 oz) over inadequate thiamine levels.
2 products
FDA•CRITICALIQF BlueberriesOregon Potato Company is recalling IQF blueberries in 30 lb. cases and 1,400 lb. totes due to potential Listeria monocytogenes contamination.
FDA•CRITICALErbe Flexible CryoprobeErbe is recalling Flexible Cryoprobes (REF 20402-401) because they may rupture or burst during activation.
4 products
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.
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•CRITICALJunebar Chocolate Cherry Snack BarJunebar Chocolate Cherry Snack Bar is recalled due to undeclared milk and soy allergens.
4 products
FDA•CRITICALWhite Vein Advanced Alkaloids Chewable TabletsShaman Botanicals is recalling White Vein Advanced Alkaloids Chewable Tablets due to higher-than-labeled levels of 7-hydroxymitragynine.
2 products
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.