FDA•MODERATE
HardyDisk Cefiderocol 30µg Susceptibility Disks
Hardy Diagnostics recalls HardyDisk Cefiderocol 30µg disks due to incorrect cartridges that may cause false susceptibility results.
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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•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
FSIS•CRITICALUkrop's Baked Spaghetti and Chicken CobblerUkrop's recalls 22,880 lbs of baked spaghetti and chicken cobbler over possible metal slivers.
4 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
FSIS•MODERATECurry Chicken SaladMary's Harvest alerts on Curry Chicken Salad due to possible Listeria; no illnesses reported.
FDA•MODERATEPower Over Fiber Base ModuleTerex Utilities recalls Power Over Fiber Base Module due to missing laser certification and improper labeling.
FDA•CRITICALAngiography Procedure Kit ManifoldsAngiography kit manifolds recalled due to particulate risk in blood circulation.
FDA•CRITICALAquafaba Powder529 Commerce recalls Aquafaba Powder over undeclared egg allergen.
FDA•CRITICALPublix Super Markets: Blueberries and Mixed BerriesPublix recalls Organic Whole Blueberries and Mixed Berries over potential E. coli O145:H28 contamination.
4 products
FSIS•MODERATERed's Steak Cilantro Lime BurritoFSIS alert: Red's Steak Cilantro Lime Burrito mislabeled, undeclared egg allergen. Do not consume if allergic.
FDA•MODERATEStryker Hoffmann II Connecting Rod Micro 3 x 30mmStryker recalls Hoffmann II Connecting Rod Micro 3 x 30mm due to potential cracking after cleaning and sterilization.
7 products
FDA•MODERATEGEM Premier 5000/7000 Bar Code Reader WandInstrumentation Laboratory recalls BCR Wand for GEM Premier 5000/7000 analyzers; may assign results to wrong patient ID.
10 products
FDA•MODERATEAzelaic Acid Gel 15%Glenmark recalls Azelaic Acid Gel 15% over grainy/gritty texture complaints.
FDA•MODERATEMellish Island Super Skin Dietary SupplementMellish Island Super Skin supplement recalled for undeclared fish allergen in marine collagen.
FDA•MODERATEOsteoBallast 45 x 17.5 mmIsoTis recalls OsteoBallast 45 x 17.5 mm DBM mesh due to underfill, risking incomplete fusion.
FDA•CRITICALResmed Astral 100/150 VentilatorResMed recalls Astral 100/150 ventilators due to supercapacitor leakage that may interrupt ventilation.
FDA•MODERATEGalliker Dairy: 2 productsGalliker recalls DQ Chocolate Reduced Fat Ice Cream Mix over possible metal shavings.
2 products
FDA•CRITICALFundamental Feed: 3 Packaged Bopp Woven Plastic WovensFundamental Feed recalls 40 lb forage pellets for horses due to elevated aflatoxin levels.
3 products
FDA•MODERATEEXO Black Tattoo InkXtreme Inks recalls EXO Black tattoo ink due to Pseudomonas aeruginosa contamination.