FDA•LOW
Pediatric PN TPN Bags
Central Admixture recalls pediatric TPN bags due to incorrect formulation.
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FDA•MODERATERed Blood Cells, Leukocytes ReducedRhode Island Blood Center recalls Red Blood Cells, Leukocytes Reduced units from a malaria-endemic-area donor.
FDA•LOWApheresis PlateletsRed Cross recalls Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced units lacking required yield testing.
FDA•MODERATEAtellica CH Urine Albumin AssaySiemens recalls Atellica CH Urine Albumin assay over falsely depressed UN_c and A1c_E results and QC failures.
2 products
FDA•MODERATEWangshin Doenjang Soybean PasteWangshin Doenjang soybean paste recalled over undeclared anchovy (fish) allergen.
FDA•MODERATEMicroScan LabPro UpdateBeckman Coulter is recalling MicroScan LabPro Update Panel Update Software Update, MicroScan LabPro Update Panel 11 (US), due to potential incorrect antibiotic resistance results that may lead to delayed or inappropriate treatment.
2 products
FDA•MODERATE5-PLASMA Bivalirudin AMR Verification KitAniara recalls 5-PLASMA Bivalirudin AMR Verification Kit (Model 5D-45905) due to stability issues causing degradation of bivalirudin.
3 products
FDA•MODERATEPhilips Allura Xper Interventional Fluoroscopic X-Ray SystemsPhilips recalls Allura Xper X-ray systems over unauthorized HDDs causing loss of imaging, movement, or data.
5 products
FDA•MODERATEHardyDisk Cefiderocol 30µg Susceptibility DisksHardy Diagnostics recalls HardyDisk Cefiderocol 30µg disks due to incorrect cartridges that may cause false susceptibility results.
FDA•MODERATEU2 Total Knee System PSA Box TrialUnited Orthopedic recalls U2 Total Knee PSA Box Trials (models 9323-5511 thru 9323-5526) due to screw defect.
4 products
FDA•CRITICALBoston Scientific Infinion CX Lead KitBoston Scientific recalls Infinion CX lead kits for SCS systems due to possible lead fracture at anchor site.
FDA•CRITICALBlank Slate Creamery Coconut Fudge SandwichesBlank Slate Creamery recalls Coconut Fudge Sandwiches due to undeclared egg allergen.
FDA•CRITICALKC Everyday Mac & CheeseKerry recalls KC Everyday Mac & Cheese over undeclared egg allergen.
FDA•MODERATEBig Way Hot Pot Miso PasteBig Way Hot Pot Miso Paste recalled for undeclared milk allergen.
FDA•MODERATEDicyclomine Hydrochloride Capsules 10mgAurobindo recalls Dicyclomine HCl 10mg capsules due to shortfill and empty capsules.
FDA•MODERATEGE Portrait Core Services Software V1.2.0GE recalls Portrait Core Services SW V1.2.0 over a security vulnerability.
2 products
FDA•MODERATEHondashi Seasoning PacketsPack'n Fresh recalls Hondashi seasoning packets due to undeclared fish allergen.
FDA•MODERATEFilmArray NGDS Warrior PanelBiofire Defense recalls FilmArray NGDS Warrior Panel due to strain mismatches affecting test accuracy.
FDA•MODERATEGE MAC VU360 ElectrocardiographGE recalls MAC VU360 ECG over software issue that may mix patient data.
FDA•MODERATEMerge PACS Medical Imaging WorkstationMerge PACS workstation recalled over risk of displaying thumbnails from a prior patient study.
2 products
FDA•LOWSyva Emit Tox Tricyclic Antidepressant Calibrator/ControlsSiemens recalls Syva Emit Tox Tricyclic Antidepressant Calibrator/Controls due to out-of-specification sodium azide concentration.
FDA•LOWSyva Emit Disopyramide AssaySiemens recalls Syva Emit Disopyramide Assay due to out-of-spec sodium azide concentration; risk of mild irritation.
FDA•CRITICALbettergoods Pistachio Nut ButterBotticelli Foods recalls bettergoods Pistachio Nut Butter over possible Salmonella contamination.
FDA•MODERATEMaquet Flow Anesthesia Machine VaporizerMaquet recalls Flow anesthesia machines over risk of insufficient anesthesia.
FDA•MODERATEIntramedullary Bone Saw Blade AssemblyBiomet recalls Intramedullary Bone Saw Blade Assembly (Model 475620) over sterile barrier damage risk.
5 products
FDA•MODERATEStryker AHTO Tube Set PackagingStryker recalls AHTO Tube Set Packaging (Cat. 0250070600) over handpiece leaking.
5 products
FDA•MODERATEDialysis Change Tray Clear SequenceMedical Action recalls Dialysis Change Tray Clear Sequence (Model 78791) due to improper seal in needle-free access device.
FDA•MODERATEOXOS MC2 Portable X-Ray SystemOXOS Medical recalls MC2 Portable X-Ray System due to overheating circuit board.
2 products
FDA•MODERATEVector Pedicle Screw System Anti-TorqueInnovasis recalls Vector Pedicle Screw System anti-torque instrument (LS-749) due to undersized tip that may prevent engagement during surgery.
FDA•MODERATEPeter Rabbit Organics Banana & Strawberry PureeCheer Pack recalls Peter Rabbit Organics Banana & Strawberry puree pouches over possible plastic strip release.
FDA•MODERATEAmerican Regent: multiple injectionsAmerican Regent recalls Adequan injections due to particulate matter including glass.
2 products
FDA•CRITICALOptiray 350 Ioversol InjectionLiebel-Flarsheim recalls Optiray 350 Ioversol Injection 500 mL vials due to particulate matter (plastic, steel, glass).
2 products
FDA•Parnell Sevoflurane 250 mLParnell recalls Sevoflurane 250 mL for dogs due to incompatible bottle notch pattern.
FDA•CRITICALHalyard Cardiac Cath Pack with Medline ManifoldAVID Medical recalls Halyard kits with Medline manifolds due to particulate risk.
3 products
FDA•MODERATEmunevo DRIVE Powered Wheelchair Control SystemMunevo recalls wheelchair control systems over software calibration issue causing steering drift and collision risk.
FDA•MODERATENerivio Infinity BatteryTheranica recalls Nerivio Infinity over battery thermal-runway risk during charging.
- Device RecallFDA•MODERATEWASPLab WebApp Software
Copan WASP recalls WASPLab WebApp software over a result-overwrite issue.
FDA•MODERATERadial Jaw 4 Biopsy ForcepsBoston Scientific recalls Radial Jaw 4 biopsy forceps due to sterile barrier breach risk.
4 products
FDA•MODERATEFORWARD Oral Airway KitIntegrated Medcraft recalls FORWARD Oral Airway Kits due to possible occluded airway tip.
2 products- Device RecallFDA•MODERATEQuantum 4Front 2 Wheelchair Controller
Quantum Rehab recalls the Quantum 4Front 2 wheelchair controller over a software issue that can cause unexpected park brake stops.
13 products 
FDA•MODERATETherabody Theragun G4 PRO ChargerTherabody recalls Theragun G4 PRO charger due to fire risk from overheating cradle.
- Device RecallFDA•MODERATEREMISOL Advance Data Manager
Beckman Coulter recalls REMISOL Advance Data Manager over software error that may misreport combo assay results.
FDA•CRITICALBD Needle Kit for Powered DriverBard Access recalls BD Powered Driver Needle Kits over obturator removal difficulty.
FDA•MODERATEUkrop's Homestyle Foods: 2 productsUkrop's recalls Bread Pudding with Vanilla Sauce due to possible metal fragments.
2 products
CPSC•EnHomee 15-Drawer DressersEnHomee 15-Drawer Dressers recalled for tip-over and entrapment hazards; violate STURDY Act.
CPSC•KAIFAM 5-Drawer DressersKAIFAM 5-Drawer Dressers recalled for tip-over and entrapment hazards; violate STURDY Act safety standards.
CPSC•BenQ GV31 Portable ProjectorsBenQ recalls GV31 portable projectors due to lithium-ion battery overheating fire and burn hazard.
CPSC•Galanz Retro RefrigeratorsGalanz recalls retro refrigerators due to fire risk; one death reported. Models BCD-215V-62H, GLR76TRDER, GLR76TBKER, GLR76TBEER, GLR76TWEER affected.
CPSC•Fantastic Four Cups and Captain America Popcorn Helmet ContainersGolden Link recalls Fantastic Four cups and Captain America popcorn helmet containers with LED lights over accessible button cell batteries posing ingestion hazard.
CPSC•Nordi Toddler Tower StoolsHARPPA recalls Nordi toddler tower stools over collapse, tip-over, and entrapment hazards.