FDA•MODERATE
KidneyVault Portable Renal Perfusion System
Paragonix recalls KidneyVault perfusion system over firmware defect causing blank screen.
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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- Device RecallFDA•MODERATEARVIS Surgical Navigation System Gen 2
Kico Knee recalls ARVIS Surgical Navigation System Gen 2 over tilted eyepiece image from sensor issue.
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.
FDA•MODERATEEndoFLIP 1 SystemCovidien recalls EndoFLIP 1 System due to 24-hour limit flagging products as expired.
2 products
FDA•MODERATEGrand Central Potato Sourdough BreadGrand Central Bakery recalls Potato Sourdough Breads due to possible metal pieces.
2 products
CPSC•COMMOWNER Pressure WashersCOMMOWNER pressure washers recalled over shock/electrocution risk due to missing GFCI and short cord.
CPSC•Cooluli MinifridgesCooluli recalls 10L and 15L minifridges due to fire and burn hazard from electrical switch short circuit.
CPSC•CuberShop Magnetic Speed CubesCuberShop Magnetic Speed Cubes recalled due to loose high-powered magnets posing ingestion hazard.
CPSC•Deli Fuel ContainersDeli fuel containers recalled; non-child-resistant closures pose burn and poisoning risks to children.
CPSC•DUMOS Nine-Drawer DressersDUMOS Nine-Drawer Dressers recalled due to tip-over and entrapment hazards; violate STURDY Act.
CPSC•Zimtown Portable Gas and Fuel CansZimtown 5-gallon gas cans recalled because non-child-resistant closures pose burn and poisoning risks.
CPSC•Merax Murphy BedsGigaCloud Technology (USA) Inc. is recalling Merax full-size and twin-size wall-mounted Murphy beds due to a frame that can fall onto consumers during assembly or disassembly, posing impact, crush, and laceration hazards.
CPSC•Goody King Magnetic Building CubesYi Suen Commerce recalls Goody King Magnetic Building Cubes over magnet ingestion hazard; full model list on CPSC page.
CPSC•Hampton Bay Halwin 52-Inch Ceiling FansHampton Bay Halwin 52-inch ceiling fans recalled due to blade separation hazard.
CPSC•Qabefy MattressesQabefy 10-inch twin mattresses recalled for violating flammability standard, posing fire risk.
CPSC•Ritchey Carbon Bicycle ForksRitchey recalls carbon bicycle forks due to loose alloy insert posing fall and crash hazard.
CPSC•Shengsen Prank Sound MakersShengsen Prank Sound Makers recalled due to accessible coin batteries posing ingestion hazard.
CPSC•Brookstone Tabletop Fire PitsBrookstone tabletop fire pits recalled due to burn and fire hazards.
CPSC•SUGIFT Pressure WashersSUGIFT recalls 2.8 GPM electric pressure washers (model LTBBHG006) over shock and electrocution hazards from missing GFCI.
CPSC•Sunnyside 1-K Kerosene ContainersSunnyside recalls 1-K kerosene containers (batch 26082) over missing flame mitigation, flash fire risk.
CPSC•Taleco Gear Baby Jumpers and SwingsTaleco Gear recalls baby jumpers and swings due to fall, impact, and strangulation hazards.
CPSC•TooyBing Wooden Bead Stacking ToysTooyBing Wooden Bead Stacking Toys recalled due to choking hazard; sold on Amazon.
CPSC•Yamazuki Youth ATVsYamazuki recalls QEASET/HOVERHEART youth ATVs (model XW-A19) over brake, speed limiter, and reflector defects posing crash hazard.
FDA•MODERATEShoolin Pharma Chem: multiple drugsShoolin Pharma Chem recalls Sildenafil and Tadalafil APIs due to CGMP deviations.
5 products
FDA•MODERATEClear Eyes Maximum Itchy Eye ReliefClear Eyes Maximum Itchy Eye Relief recalled over potential sterility issues.
FDA•MODERATERed Blood Cells, Leukocytes ReducedRed blood cell units distributed after donor tested reactive for hepatitis C antibody.
- FDA•MODERATERed Blood Cells, Leukocytes Reduced
Hoxworth recalls Red Blood Cells, Leukocytes Reduced due to malaria risk from donor travel.
FDA•MODERATEPresource KitsCardinal Health is recalling multiple Presource procedural kits due to possible endotoxin contamination.
13 products
FDA•MODERATEBD Intravascular Administration and Extension SetsBD recalls IV administration and extension sets due to possible sterilization failure.
2 products
FDA•MODERATEMarketside Tomato Bisque Soup KitMarketside Tomato Bisque Soup Kit recalled due to possible Listeria contamination.
- FDA•MODERATEApheresis Red Blood Cells, Leukocytes Reduced
LifeShare Blood Centers recalls apheresis red blood cells, leukocytes reduced, from a donor with incomplete eligibility screening.
FDA•MODERATERed Blood Cells, Leukocytes ReducedLifeShare distributed leukoreduced red blood cells from a malaria-endemic-area donor.
FDA•MODERATEERBECRYO 2 Cryosurgical UnitErbe USA recalls ERBECRYO 2 Cryosurgical Unit (Model 10402-000) over risk of cryoprobe rupture from CO2 leak.
FDA•MODERATEProNephro AKI (NGAL) Reagent KitBioporto recalls ProNephro AKI (NGAL) Reagent Kit over non-validated rework that could cause missed renal disease diagnosis.
FDA•MODERATEBIOFIRE Respiratory Panel 2.1BioFire recalls BIOFIRE Respiratory Panel 2.1 over increased false negatives.
FDA•MODERATESchwarzkopf Professional Osis Grip MousseHenkel recalls Schwarzkopf Osis Grip Mousse 6.76 oz cans over explosion risk from packaging leak.
FDA•MODERATEStraumann Bone Level Tapered ImplantStraumann recalls BLT Implant D 4.1mm RC SLActive 14mm due to possible 12mm length mismatch.
FDA•MODERATEEndo-Model Tibial Plateau Replacement SetWaldemar Link recalls Endo-Model tibial plateau replacement sets that may contain the wrong hinge component.
FDA•MODERATEClindamycin Palmitate Hydrochloride Oral SolutionAvet recalls Clindamycin Palmitate Oral Solution 75 mg/5 mL over particles and white flakes.
FDA•MODERATEER-Spec Vaginal SpeculumOBP Medical recalls ER-Spec X-Small vaginal speculums over a sharp-edge burr risk.