FDA•
Morasch Meats: 2 Raw Frozen Net Weight Packageds
Northwest Naturals raw cat and dog diets recalled over Salmonella risk.
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FDA•MODERATEPaxil CR Paroxetine 37.5mg TabletsApotex recalls Paxil CR 37.5mg tablets for failing dissolution specs.
FDA•MODERATERamipril Capsules USP 10 mgHikma recalls Ramipril Capsules USP 10 mg over a failed impurity (DCU) specification.
FDA•MODERATEByron White Formulas: 3 May Contain Nuts CasByron White Formulas recalls A-L Complex, A-FNG, and A-P herbal supplements due to undeclared walnuts.
3 products
FDA•MODERATEOlympus PowerSeal 5 mm Curved Jaw Sealer & DividerOlympus recalls PowerSeal 5 mm Curved Jaw Sealer & Divider over labeling error.
FDA•MODERATEZicam Medicated Nasal SwabsZicam nasal swabs recalled over microbiological testing failures.
FDA•MODERATEIMRIS ORT200 Operating Room TableIMRIS recalls ORT200 operating room tables due to actuator/lock failure risk of unintended movement.
2 products
FDA•MODERATEActhar Gel (Repository Corticotropin Injection) 5 mL VialsMallinckrodt recalls Acthar Gel 5 mL vials over glass and stopper particulate.
2 products
FDA•MODERATEClobetasol Propionate Cream USP, 0.05%Lupin recalls Clobetasol Propionate Cream 0.05% due to failed content uniformity.
FDA•MODERATEhealthmark ProChek-II TestHealthmark recalls ProChek-II tests (PT-313, PT-201-12) over expired ingredient risk.
2 products- Device RecallFDA•MODERATEFUJIFILM Synapse PACS Software
FUJIFILM Synapse PACS v7.4.310 recalled due to inaccurate ruler measurements.
FDA•MODERATEMedline Femoral Pack and FEVAR KitsMedline recalls Femoral Pack and FEVAR kits due to potentially contaminated component.
14 products
FDA•MODERATEGENESYS CrossFT Suture AnchorConMed recalls GENESYS CrossFT Suture Anchor (REF CFBC-5502B) due to incorrect implant card.
FDA•MODERATEFresenius 2008T BlueStar Hemodialysis MachineFresenius recalls 2008T BlueStar Hemodialysis Machine over flow, no water, and temperature alarms.
FDA•MODERATEStructur 2 SC Temporary Resin Cartridge RefillHenry Schein recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm due to incorrect packaging and IFU.
2 products
FDA•MODERATEMidmark IQecg Digital ECGMidmark recalls IQecg Digital ECG over incorrect ECG waveforms and BPM calculations.
2 products
FDA•MODERATECanon Alphenix Ceiling Movement Gear ScrewsCanon recalls Alphenix X-ray systems (INFX-8000C/F/V) over loose ceiling gear screws.
FDA•MODERATELevothyroxine Sodium Tablets 25 mcgAccord recalls Levothyroxine 25 mcg tablets due to subpotency.
12 products
FDA•MODERATEHalyard Davinci TruCustom Foley TrayHalyard Davinci TruCustom Foley tray recalled over missing latex warning on StatLock component.
8 products
FDA•MODERATEMerge PACS and Merge OrthoPACSMerge PACS and OrthoPACS recalled due to inaccurate measurement display.
FDA•MODERATEAmerican Contract System Convenience KitAmerican Contract Systems recalls Convenience Kit CV B PACK (TNCB10AM) due to catheter performance failure.
4 products- Device RecallFDA•MODERATEPhilips Incisive CT Software
Philips Incisive CT software V4.5/V5.0 recalled for Bolus Tracking scan trigger failure.
FDA•MODERATEMedline Trach Tube KitMedline recalls Trach Tube Kit (SKU DYKM2330) over labeling discrepancy.
FDA•MODERATEOnli Hydrophilic Urethral Intermittent CathetersHollister recalls Onli intermittent catheters due to a protrusion defect that may cause genitourinary trauma or bleeding.
2 products
FDA•MODERATEMedline ENT Convenience KitsMedline recalls ENT/sinus kits with Pilling Wecksorb Neurosponges over endotoxin risk.
6 products
FDA•Glutathione 200 mg/mL Sterile Multidose VialsOptimal Balance Pharmacy recalls Glutathione 200 mg/mL vials over bacterial endotoxin contamination.
FDA•MODERATECarbamazepine Tablets 200mgGSMS recalls Carbamazepine 200mg tablets over black specks.
FDA•MODERATEAcamprosate Calcium 333 mg TabletsMylan recalls Acamprosate Calcium 333 mg tablets over dissolution failure.
FDA•MODERATEEsteem Body Soft Convex Urostomy PouchConvaTec recalls Esteem Body Soft Convex Urostomy Pouches due to cap leakage risk.
FDA•MODERATEVeritas Standard Glenoid Baseplaterestor3d recalls Veritas Standard Glenoid Baseplate over screw hole machining defect.
2 products
FDA•MODERATECarbamazepine Tablets 200mgTaro recalls Carbamazepine 200mg tablets over black specks.
2 products
FDA•MODERATEFDI Automated Field Steam SterilizerFDI recalls Automated Field Steam Sterilizer over possible ground continuity loss in the water recovery system connector.
FDA•MODERATESyva EMIT 2000 Quinidine AssaySiemens recalls Syva EMIT 2000 Quinidine Assay over precision issues that may cause elevated readings and risk of cardiac arrhythmias.
2 products- Device RecallFDA•MODERATEBeckman Coulter DxC 500i Analyzer Modules
Beckman Coulter recalls DxC 500i Analyzer Modules (software ≤1.5) over a Parameter Package import defect that can yield erroneous results.
2 products 
FDA•MODERATEProtein Cereal Cocoa CrunchProtein Cereal Cocoa Crunch recalled over undeclared soy allergen.
FDA•MODERATEPEMRYDI RTU Pemetrexed InjectionShilpa Medicare recalls PEMRYDI RTU vials over green discoloration.
2 products
FDA•MODERATELibtayo (cemiplimab-rwlc) InjectionRegeneron recalls Libtayo (cemiplimab-rwlc) Injection 350 mg/7 mL over sterility concerns.
FDA•MODERATEGentherm Thermal Regulating SystemGentherm recalls thermal regulating systems over CPU board overheating that may cause shutdown.
3 products
FDA•MODERATEKidneyVault Portable Renal Perfusion SystemParagonix recalls KidneyVault perfusion system over firmware defect causing blank screen.
FDA•MODERATESiemens Healthineers Immulite 2000 SYP Syphilis ScreenSiemens Healthineers recalls Immulite 2000 SYP Syphilis Screen due to negative bias risk.
2 products
FDA•MODERATEHalyard LAVH Pack Clearify Visualization SystemAVID Medical recalls Halyard LAVH Pack (USAR053-11) due to possible leakage of the Clearify Visualization System.
2 products
FDA•MODERATEGetinge SERVO-U/SERVO-N Y Sensor ModuleGetinge recalls SERVO-U/N Y sensor module over missing safety electrical testing.
2 products
FDA•MODERATEOverStitch Suture CinchBoston Scientific recalls OverStitch Suture Cinch over deployment and suture-cutting failures.
2 products
FDA•MODERATEProspector Popcorn: 4 productsProspector Popcorn recalls gourmet popcorn varieties over inaccurate nutrient declarations.
4 products
FDA•MODERATETD Navio Midi Speech Generating DeviceTobii Dynavox recalls TD Navio Midi speech device over battery tab damage risk.
2 products
FDA•MODERATEArrow-LOK ImplantArrowhead recalls Arrow-LOK Implants over missing gamma radiation audit, risking infection.
2 products
FDA•MODERATEPhilips Cardiac Workstation 5000Philips recalls Cardiac Workstation 5000 over intermittent inaccurate heart-rate data.
2 products
FDA•MODERATEDentsply Sirona Capsule MixerDentsply Sirona Capsule Mixer recalled over electrical discharge risk when unplugged.
FDA•MODERATEIntersurgical One-Piece Guedel AirwayIntersurgical recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue, due to potential occlusion.
2 products- Device RecallFDA•MODERATEHamilton Microlab STAR PCT Software
Foundation Medicine recalls Hamilton Microlab STAR PCT v2.0.0 over spontaneous software closures.