Archive
472 recalls were announced in August 2026.
Of the 472 recalls this month scored against our rubric, 12% are Critical, 34% are Severe.
Which agencies issued them
Spectral Instruments Inc is recalling 40 Lago X units because the 'X-Ray On' banner may briefly disappear during the run readiness check.
FDA is recalling 327 EndoFLIP Systems because a software error incorrectly flags catheters as expired, making them unavailable for clinical procedures.
Mylan Pharmaceuticals is recalling Acamprosate Calcium tablets that failed to meet dissolution specifications.
Prospector Popcorn is recalling 21,400 units of Maple Walnut Ice Cream Gourmet Popcorn due to inaccurate nutrient declarations for potassium, calcium, and iron.
Prospector Popcorn is recalling Belgian Chocolate Toffee Gourmet Popcorn due to inaccurate nutrient declarations for Iron and Vitamin D.
Paragon 28, Inc. is recalling a custom-made foot implant due to elevated oxygen levels that may reduce material ductility.
Ford is recalling 2024-2026 Mustangs because engine compartment wiring harness ground connections may fracture, potentially causing loss of drive power or essential vehicle functions.
Ford is recalling 2026 Explorer, Bronco, Bronco Sport, Mustang, and Ranger vehicles because incorrectly manufactured engine piston domes may fail, causing a loss of drive power.
Ford is recalling 2026 Maverick, F-150, and Bronco Sport vehicles because improperly tightened joints may lead to detached parts or loss of vehicle control.
Mitsubishi is recalling 2025-2026 Outlander and 2026 Outlander PHEV vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.
Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER EFX2 and HDX2 school buses because missing connector plates may compromise seat belt anchorages and body joint strength.
Rennline Automotive is recalling 106 lower control arms that may have incorrect dimensions, potentially damaging the subframe and causing loss of steering control.
PACCAR is recalling 811 specific 2027 Kenworth and Peterbilt trucks because a missing heat-shrink on the seat ventilation harness may cause a short circuit and fire.
T.A. Pelsue is recalling 2024-2025 Fost XL, FiberLite, and MPCCT trailers because axle mounting brackets may crack and fail, increasing crash risk.
Cornell Pump is recalling 2025 Utility and Enclosed Pump Trailers because a cracked tongue may cause instability and increase crash risk.
Altec is recalling specific aerial devices and digger derricks because the automatic braking system was not recalibrated after moving the front radar box, increasing crash risk.
Kia is recalling 2025-2026 EV9 vehicles because the Occupant Detection System may fail to deactivate the front passenger air bag for child seats.
Modine is recalling Airedale ventilation fans in specific school heat pumps because water exposure can cause short circuits and fires. No injuries have been reported.
Rossmonster is recalling 2026 Baja, Skye, and Havn motorcoaches because a rooftop ventilation fan component may overheat and cause a fire.
Workbless is recalling electric pressure washers models WB0301 and WB0302 due to risks of serious injury or death from shock and electrocution.
CPSC recalls JINHEZO Mini Waterproof LED Tea Lights because accessible button batteries pose a serious injury or death risk if swallowed.
KTM North America is recalling approximately 21,040 GASGAS and Husqvarna off-road motorcycles because the rear brake caliper can crack or break, posing a crash risk.
Goal Zero is recalling about 46,200 YETI 3000X portable power stations because the circuit board can overheat, posing a risk of fire and burn injuries.
Lucid is recalling 2022-2026 Air vehicles because an electrical circuit may overheat, increasing the risk of fire or reduced visibility.
General Motors is recalling 2024-2026 Buick and Chevrolet SUVs because the rearview camera may display a distorted or blank image, increasing crash risk.
CPSC recalls Koorlian mattresses sold on Amazon due to fire risks from violating mandatory flammability standards. Consumers should stop using them and contact the manufacturer for a free cover.
CCM Hockey is recalling FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories because they can crack upon impact, posing a risk of laceration or impact injury.
Britax is recalling specific infant car seats because a screw in the carrying handle may come loose, causing the handle to partially detach and increasing the risk of a child falling.
Marathon Industries is recalling one 2025 Ford F-650 SD because deck pins may break, causing the liftgate platform to fall and increasing injury risk.
Taylor Farms de Mexico is recalling Jack in the Box shredded lettuce products due to potential Cyclospora contamination.
Taylor Farms is recalling Cross Valley Farms lettuce salad mix products due to potential Cyclospora contamination.
Midwest Poultry Services is recalling 1.59 million dozen eggs due to possible Salmonella Enteritidis contamination. The recall affects Kroger, Brookshire's, and Country Morning brands in six states.
Taylor Farms is recalling Markon Lettuce Salad Mix products due to potential Cyclospora contamination. The recall affects 1,575 cases distributed across 28 US states and Mexico.
Victory Medical Center Pharmacy is recalling 91 vials of Glutathione (MDV) 200 mg/mL due to bacterial endotoxin contamination.
Taylor Farms is recalling specific bags of lettuce salad due to potential Cyclospora contamination. The products were distributed to 28 U.S. states and Mexico.
Buy-Herbal is recalling Kian Pee Wan Capsules because they contain undeclared dexamethasone and cyproheptadine. The product was sold to consumers via an eBay third-party seller.
Taylor Farms is recalling specific lots of Sysco lettuce salad mix due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.
Bazzini LLC is recalling Dark Chocolate Coconut Almond Bites distributed in Washington due to undeclared peanuts, a major food allergen.
Midwest Poultry Service is recalling 1.59 million dozen Simple Truth and bulk eggs due to a possible Salmonella Enteritidis contamination.
Liebel-Flarsheim is recalling 3,486 vials of Optiray Injection due to the presence of particulate matter, including plastic, stainless steel, and glass.
Taylor Farms is recalling specific iceberg lettuce products due to potential Cyclospora contamination. The recall affects 16,314 cases distributed across 28 US states and Mexico.
Piazza Produce is recalling Garden Salad products due to possible Cyclospora contamination. The recall affects 1,279 units sold in six states.
Taylor Farms de Mexico is recalling Cross Valley Farms lettuce blends due to potential Cyclospora contamination. The products were distributed to multiple US states and Mexico.
Taylor Farms is recalling specific Peak Lettuce Salad products due to potential Cyclospora contamination. Consumers should check for specific codes and stop eating the product.
Taylor Farms de Mexico is recalling specific lots of shredded iceberg lettuce due to potential Cyclospora contamination. The product was distributed to 28 U.S. states and Mexico.
Taylor Farms is recalling specific lots of Cross Valley Farms iceberg lettuce due to potential Cyclospora contamination. The products were distributed across 28 US states and Mexico.
Taylor Farms is recalling specific Markon iceberg lettuce products due to potential Cyclospora contamination. Consumers should check lot codes and stop using affected items.
Taylor Farms is recalling pre-blended lettuce products due to potential Cyclospora contamination. The recall affects 1,161 cases distributed across 28 US states and Mexico.
Taylor Farms is recalling specific lots of chopped and shredded iceberg lettuce due to potential Cyclospora contamination. The products were distributed to 28 states and Mexico.
Taylor Farms de Mexico is recalling specific lots of mixed lettuce products due to potential Cyclospora contamination. The products were distributed to 28 U.S. states and Mexico.
Taylor Farms de Mexico is recalling specific lots of Sysco blend lettuce products due to potential Cyclospora contamination. The recall affects 1,834 cases distributed across 28 US states and Mexico.
Baxter Healthcare is recalling 24,528 units of Duo-Vent Solution Sets due to customer reports of air bubbles in the drip chamber and tubing.
Taylor Farms is recalling specific Cross Valley Farms lettuce products due to potential Cyclospora contamination. Consumers should check lot codes and discard or return affected items.
Taylor Farms is recalling specific Marketside iceberg salad products due to potential Cyclospora contamination. Consumers should check lot codes and discard affected items.
529 Commerce, LLC is recalling Aquafaba Powder, Vegan Replacement, because it contains undeclared egg. The product was distributed to 24 states.
FDA is recalling Surgipro II sutures due to potential sterile packaging defects that could cause biocontamination and infection.
Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.
Prestige Brands Holdings is recalling Clear Eyes Maximum Itchy Eye Relief eye drops due to a lack of assurance of sterility and potential contamination.
Baxter Healthcare is recalling 19,032 bags of Cefazolin Injection due to the presence of particulate matter. The affected product is distributed nationwide in the US.
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.
Erbe USA Inc is recalling ERBECRYO 2 Cryosurgical Units because a strong pull on the high-pressure transfer hose may cause the cryoprobe to rupture.
Apollo Care, LLC is recalling 56,918 vials of Semaglutide 12.5mg due to the presence of nylon and silk particulate matter.
Apollo Care, LLC is recalling 250 vials of Semaglutide 5mg due to the presence of nylon and silk-type particulate matter.
Apollo Care, LLC is recalling specific lots of Semaglutide 20mg vials because they contain nylon and silk-type particulate matter.
Taylor Farms is recalling specific lots of Subway Shred Lettuce due to potential Cyclospora contamination. The product was distributed to 28 US states and Mexico.
Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.
Spectra Medical Devices is recalling Sodium Chloride Injection ampules because manufacturing issues may have compromised sterility, posing a risk of infection or inflammation to patients.
Apollo Care, LLC is recalling 9,762 vials of Semaglutide 4.5mg due to the presence of nylon and silk-type particulate matter.
Apollo Care, LLC is recalling 500 vials of Semaglutide 10mg due to the presence of nylon and silk-type particulate matter.
Apollo Care, LLC is recalling 250 vials of Semaglutide 2.5mg due to the presence of nylon and silk particulate matter.
Apollo Care, LLC is recalling specific lots of Semaglutide 2.25mg vials because they contain nylon and silk-type particulate matter.
Taylor Farms is recalling specific lots of garden salad mix and lettuce blends due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.
Taylor Farms de Mexico is recalling specific lots of shredded iceberg lettuce due to potential Cyclospora contamination. The product was distributed across 28 U.S. states and Mexico.
Shoolin Pharma Chem LLP is recalling Tadalafil USP 1.00 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Taylor Farms de Mexico is recalling specific lots of iceberg and romaine lettuce blends due to potential Cyclospora contamination.
Covidien is recalling Dermalon 4-0 sutures because sterile barrier packaging may be perforated or torn, risking biocontamination and infection.
Apollo Care, LLC is recalling specific lots of Semaglutide 9mg vials because they contain nylon and silk-type particulate matter.
SHEANDRO LLC is recalling Vodka Tomato Sauce because the label declares cream and cheese but fails to declare milk, a major allergen.
FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.
Bioporto Diagnostics is recalling ProNephro AKI Reagent Kits because a non-validated rework process could lead to missed diagnoses of renal disease.
Avride Inc. is recalling Automated Driving Systems (ADS) with specific software versions that may cause unsafe lane changes or merging without yielding.
BD Switzerland is recalling 93,700 intravascular extension sets because they may not have received adequate sterilization processing.
Covidien, LP is recalling V-Loc 90 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that may cause biocontamination.
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because bleach concentration may drop below specification, potentially compromising disinfection effectiveness.
FDA is recalling Surgipro sutures due to potential sterile barrier defects that could cause biocontamination and infection.
Cardinal Health is recalling 616 Presource Kits because they contain sponges with unexpected endotoxin variability.
Waldemar Link is recalling Endo-Model tibial plateau replacement sets that incorrectly contain a Pure Hinge plateau, posing a risk of increased wear if implanted.
Cardinal Health 200, LLC is recalling 52,699 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.
Microvention Inc. is recalling 5,500 Bobby Balloon Guide Catheters worldwide due to an increased rate of balloon pinhole defects.
Medline is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness, potentially allowing pathogenic microorganisms to survive.
Philips is recalling 4,252 Allura Xper FD interventional fluoroscopic x-ray systems worldwide due to a firmware issue that may cause loss of geometry movements.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Philips is recalling 2,016 Azurion interventional fluoroscopic x-ray systems worldwide due to software defects that may degrade image quality or lose geometry movements, potentially delaying therapy or causing procedural complications.
Cardinal Health is recalling specific Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Medline is recalling bleach wipes that may lose potency before expiration, potentially allowing pathogens to survive.
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness.
Philips is recalling Azurion Rystem X-ray systems due to software defects that may degrade image quality or lose geometry movements, potentially delaying therapy or causing procedural complications.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Cardinal Health is recalling 602 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.
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