Hawaii recalls

Sold nationwide. Fromm Family Foods is recalling two wet dog food products: Turkey Pâté and Diner Classics Milo's Meatloaf Pâté, sold in 12.2 oz. and 12.5 oz. cans with a Best By date of 032029. The recall is due to potential metal contamination discovered during production. If dogs eat metal, they can choke, vomit, lose appetite, or suffer cuts and blockages in the mouth or digestive tract.

Serious·FDA·Aug 21, 2026·Fromm

Sold nationwide. CCM Hockey visors and replacement visor accessories can crack when hit during play, potentially causing cuts or impact injuries. The recalled products are FMHVR Hybrid Visors and ACCHVR Replacement Visor accessories with specific serial numbers.

Serious·CPSC·Aug 20, 2026·CCM

Sold nationwide. Workbless pressure washer models WB0301 and WB0302 lack proper electrical safety features—specifically a ground-fault circuit-interrupter (GFCI) and an adequate power cord. This creates a serious risk of electric shock or electrocution during use.

Serious·CPSC·Aug 20, 2026·Workbless

Sold nationwide. Koorlian brand mattresses sold on Amazon do not meet federal flammability safety standards and pose a serious fire risk. The recalled mattresses are 10 inches thick, Twin XL size, with white tops and blue sides, and were sold compressed in boxes between November 2025 and March 2026.

Serious·CPSC·Aug 20, 2026·Dreams Bedding Technology

Sold nationwide. These small LED tea lights contain button-cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal injuries, chemical burns, and death. The product also lacks required safety warnings.

Serious·CPSC·Aug 20, 2026·Mystic ZO

Sold nationwide. The circuit board in Goal Zero's YETI 3000X power stations can overheat, which may cause the unit to catch fire or smoke. Goal Zero has received four reports of units catching fire or overheating, though no injuries have been reported so far.

Serious·CPSC·Aug 20, 2026·Goal Zero

Sold nationwide. The ventilation fan motor in Modine's Airedale heating and cooling units can short circuit if water reaches the circuit board, causing the units to overheat and potentially catch fire. The affected models are ClassMate and SchoolMate heat pumps installed in schools and classrooms since 2013. Modine has received 11 reports of fires causing over $2.7 million in property damage.

Serious·CPSC·Aug 20, 2026·Modine

Sold nationwide. The rear brake caliper on certain 2021–2024 Husqvarna and GASGAS off-road motorcycles can crack or break, which reduces braking power and increases the risk of a crash. About 21,040 motorcycles are affected. No injuries have been reported so far.

Serious·CPSC·Aug 20, 2026·KTM

Sold nationwide. Optimal Balance Pharmacy identified elevated bacterial endotoxin levels in one lot of compounded glutathione 200 mg/mL multi-dose vials during testing. Endotoxins can cause fevers, low blood pressure, severe allergic reactions, and in serious cases, death. The pharmacy has already received reports of adverse events including fever, chills, severe headache, nausea, vomiting, and allergic-like reactions.

Serious·FDA·Aug 19, 2026·Optimal Balance Pharmacy

Sold nationwide. B. Braun Medical Inc. is recalling one lot of Excel Lactated Ringers Injection (1000mL) distributed to hospitals and healthcare facilities because the solution contains small particles—primarily cellulose fibers from cotton, wood, and polystyrene. These particles could cause blood clots, vein inflammation, or organ damage if infused intravenously. No injuries have been reported so far.

Serious·FDA·Aug 19, 2026·Excel

Sold nationwide. Cardinal Health is recalling 8 Presource procedure kit product groups, sold under the Cardinal Health Presource Kits name, that contain MEDICOM Ritmed Neurological Sponges. The sponges had unexpected variability in endotoxin levels. The kits were distributed across the US and to Canada, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Cardinal Health8 products

Sold nationwide. Erbe USA is recalling certain ERBECRYO 2 cryosurgical units because a strong pull on the high-pressure transfer hose can cause CO2 to leak into the return path. The resulting excess pressure may rupture the cryoprobe. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Erbe

Sold nationwide. Bioporto Diagnostics recalled certain lots of the ProNephro AKI (NGAL) Reagent Kit, a test used to help detect acute kidney injury. The reagents were reworked using a process that had not been validated, which could lead to missed kidney disease, incorrect treatment decisions, or inappropriate monitoring. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Bioporto Diagnostics

Sold nationwide. BioFire Diagnostics is recalling certain lots of its BIOFIRE Respiratory Panel 2.1 (RP2.1) test, a lab test that detects respiratory infections. The company found an increase in false negative results, meaning the test can miss an infection that is actually present. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·BioFire Diagnostics

Sold nationwide. Straumann USA is recalling one lot of its Bone Level Tapered (BLT) dental implants, 14mm model, because some may actually be 12mm long, which does not match the label. The recall covers 175 units distributed nationwide, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Straumann

Sold nationwide. OBP Medical is recalling certain lots of its ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small size, because the plastic blade may have a burr that could create a sharp edge. The edge could contact both the patient and the healthcare provider. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·OBP Medical

Sold nationwide. Philips is recalling certain Azurion interventional fluoroscopic X-ray systems, model numbers 722229 through 722236, running software versions R3.0 and R3.1. The software can degrade image quality, and it can also cause loss of geometry movements, which may delay treatment or complicate procedures. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Philips

Sold nationwide. Philips is recalling certain Azurion interventional fluoroscopic X-ray systems running software version R2.2.10. The software can degrade image quality or cause a loss of geometry movements, which may delay treatment or lead to procedural complications. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Philips

Sold nationwide. Terumo Medical Corporation is recalling certain GlideSheath Slender A-Kit 6F 10cm .021GW kits (Product Code 60-1060) because they were packaged with a 0.025 guidewire instead of the labeled 0.021 guidewire. The kit is used to help place a catheter through the skin into the radial artery. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Terumo

Sold nationwide. Straumann USA is recalling certain GM Helix dental implants (Article No. 109.984, Lot MVXJ9) because the implant inside the package may not match the outer carton label. If the wrong implant is placed, it could cause bone compression or make installation difficult where there is sufficient bone. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Straumann

Sold nationwide. Philips Medical Systems recalled certain Allura Xper FD interventional fluoroscopic X-ray systems, affecting about 4,252 units. A firmware problem may cause the system to lose some geometry movements. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Philips

Sold nationwide. Certain lots of the Remel (Thermo Fisher Diagnostics) Neisseria meningitidis Group C 2 mL test, product R30166901, did not perform as its instructions require. The test did not return a positive result with a reference control strain within 60 seconds. About 26 units were distributed nationwide, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Remel

Sold nationwide. Medline is recalling four sizes of Micro-Kill Bleach Germicidal Bleach Wipes, about 1.07 million units in total. The bleach concentration in the wipes may drop below the labeled level before the 12-month shelf life ends, which could reduce their ability to kill germs.

Moderate·FDA·Aug 19, 2026·Medline4 products

Sold nationwide. Covidien is recalling five surgical suture products, including V-Loc 90, V-Loc 180, Dermalon, Surgipro and Surgipro II, with about 135,875 units affected. The sterile packaging may have a tear or hole, which could let germs reach the sutures and cause infection, prolonged surgery, or vision loss if used in eye surgery. The recall covers the US and many other countries, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Covidien5 products

Sold nationwide. Black depth markings on the outer sheath of the coaxial dilator introducer in certain Boston Scientific Enhance transcarotid and peripheral access kits may detach. The recall covers about 114,260 kits across many lot numbers. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Galt Medical

Sold nationwide. Spacelabs Healthcare is recalling about 6,074 Xhibit Central Station units, model 96102, which are used to remotely monitor patient data. The recall involves a third-party DisplayPort audio/video splitter that can fail, interrupting audio and video output to extra displays. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Spacelabs Healthcare

Sold nationwide. Some GORE VIABIL Short Wire Biliary Endoprosthesis devices labeled as model VSWVN1010 (10 mm by 10 cm, without transmural drainage holes) are actually model VSWVH1006 (10 mm by 7 cm, with transmural drainage holes). The recall covers 13 units, sold in Georgia and Rhode Island, and no injuries have been reported. The device is used to keep the common bile duct open when it is blocked.

Moderate·FDA·Aug 19, 2026·Gore2 products

Sold nationwide. Ventana Medical Systems is recalling navify Digital Pathology software, version 2.5, used with the Roche Digital Pathology Dx slide imaging system. Customers reported that images did not match their information (metadata) in the viewer window. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Ventana Medical Systems

Sold nationwide. MicroVention is recalling certain BOBBY Balloon Guide Catheters because the balloons may develop pinhole defects, which occur at an increased rate. The catheter is used by health care providers to guide a catheter into blood vessels during peripheral and neurovascular procedures. The FDA has classified the recall as Class II, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Microvention

Sold nationwide. Baxter Healthcare is recalling certain Duo-Vent solution sets (product code 1C8507) because air bubbles can form in the drip chamber and tubing. Customers reported this happening when a pressure cuff was in use or when the tubing was flushed with the clamp fully open. About 24,528 units were distributed nationwide, and no injuries have been reported.

Serious·FDA·Aug 19, 2026·Baxter