FDA•MODERATE
Levothyroxine Sodium Tablets USP 150 mcg
Macleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.
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FDA•MODERATENomida Semaglutide InjectionNew Life Pharma is recalling Nomida Semaglutide Injection due to a lack of assurance of sterility.
4 products
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsLowes Foods sour cream and onion potato chips recalled for inaccurate nutrition labels and undeclared MSG.
FDA•MODERATESynthes 2.4 Volt Locking Screw TapSynthes is recalling the 2.4 Volt Locking Screw Tap due to a labeling error that resulted in the inclusion of incorrect thread components.
2 products
FDA•MODERATEOlympus PKS Cutting ForcepsOlympus is recalling PKS Cutting Forceps (model 3005PK) because defective welds may cause the device's jaw to break during use.
7 products
FDA•MODERATEMedline Namic GuidewiresMedline is recalling 50+ variants of Namic Guidewires due to the rescission of their 510(k) regulatory clearances.
28 products- Food RecallFDA•MODERATEGreenway Farms Jalapeno Dill Pickle Chips
Greenway Farms is recalling 16 fl oz Jalapeno Dill Pickle Chips due to the lack of a required process authority.
2 products 
FDA•MODERATEKing Harvest HummusKing Harvest is recalling Jalapeno and Roasted Red Pepper Hummus in 10 oz and 17 oz tubs due to potential aluminum piece contamination.
6 products
FDA•MODERATEImu-Tek Colostrum-5 CapsulesImu-Tek is recalling Colostrum-5 dietary supplement capsules due to the product being potentially under-processed.
2 products
FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
FDA•MODERATEStryker CHROMOPHARE Softlit Ring Surgical LightStryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential failure of the ceiling cover support assembly.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c (A1c_E)Siemens is recalling Atellica CH A1c_E assays due to a risk of depressed results when processed alongside RCRP on the same analyzer.
FDA•MODERATEGreat Value Fat Free Cottage CheeseSaputo Cheese is recalling Great Value Fat Free Cottage Cheese due to potential under-pasteurization.
5 products
FDA•MODERATEElegance Anterior Cervical PlateClariance-SAS is recalling Elegance Anterior Cervical Plates due to the presence of burrs on the finished product.
2 products
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•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•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•MODERATEAptima HPV AssayHologic is recalling the Aptima HPV assay (catalog 303585) due to the potential for 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•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•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.
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.
FDA•MODERATEFrozen Cooked Medium ShrimpH & N Group is recalling 1 lb bags of frozen cooked medium shrimp due to potential Cesium-137 contamination.