Archive
472 recalls were announced in August 2026.
Of the 472 recalls this month scored against our rubric, 12% are Critical, 31% are Severe.
Which agencies issued them
Tiffin is recalling 2026-2027 Wayfarer recreational vehicles because the liquid propane tank may lack a remote shut-off or be loose, posing fire and crash risks.
Tesla is recalling 2026 Model Y vehicles because front suspension fasteners may not be properly tightened, which could cause a loss of vehicle control.
Jayco is recalling 2026-2027 Entegra and Seneca recreational vehicles because the tire size on the certification label may be incorrect, which could lead to installing the wrong replacement tires.
Jayco is recalling certain 2027 Entegra Qwest and Jayco Melbourne Prestige recreational vehicles due to a taillight harness defect that may cause incorrect warning lights on the instrument panel.
Blue Bird is recalling 2025-2027 Vision school buses because a faulty electrical contactor may prevent wheelchair lifts from stopping, increasing injury risk.
Magic Tilt is recalling 2025-2026 aluminum watercraft trailers because the winch weld may fail, causing the winch to detach and potentially injure nearby people.
Jayco is recalling 2027 Heartland Bighorn recreational trailers because the Gross Axle Weight Rating on the certification label may be incorrect, potentially leading to overloading.
Steelite electric pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing a risk of serious injury or death.
YERYORK pressure washers are recalled because they lack a ground-fault circuit-interrupter, posing a risk of shock or electrocution.
Kmaier recalls infant walkers that violate safety standards by failing to stop at step edges, posing a risk of serious injury or death.
AudioLineOut is recalling Studio Six Headphone Amplifiers because they pose a risk of serious injury or death from electrocution when used with aftermarket metal base tubes.
CPSC is recalling Chillife 5-in-1 Montessori Baby Toy Sets because the pull string teething toy violates safety standards and poses a choking risk to children.
Altec is recalling 2021-2023 Service Body vehicles because water leaks into strobe lights, causing electrical short-circuits that increase fire risk.
Conair is expanding a recall of over 3.6 million Cuisinart grill brushes because metal wire bristles can detach and be swallowed, posing a risk of serious internal injury.
Walmart is reannouncing a recall of Mainstays 9-Drawer Fabric Dressers because they pose tip-over and entrapment hazards that can cause serious injury or death to children.
HABA USA is recalling Rainbow Rattle Grasping and Teething Toys because a glued knot can untie, exposing small parts that pose choking and ingestion risks to young children.
Little Loves & Co. is recalling youth clothing sets with drawstrings due to an entrapment hazard that could cause serious injury or death to children.
Diamond Wipes International is recalling MD Wipe Outz Numbing Tattoo Wipes because the packaging is not child-resistant, posing a risk of serious injury or death from child poisoning.
Excel Industries is recalling about 1,800 accessory LED light kits for Hustler and BigDog ride-on mowers because the light bars can overheat or produce flames.
Coast Citrus Distributors is recalling bulk jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed to wholesale distributors and has not been sold at retail.
American Regent, Inc. is recalling Papaverine Hydrochloride Injection due to the presence of glass and/or paraformaldehyde particulate matter.
Publix Super Markets is recalling Organic Whole Mixed Berries due to potential E. coli O145:H28 contamination. The product was distributed in eight southeastern states.
Whole Foods Trio Dip is being recalled because the jalapeños used in the product may be contaminated with Salmonella.
Whole Foods Market is recalling Mild Guacamole Dip because it was made with jalapenos that may be contaminated with Salmonella.
Dairyland Produce, LLC is recalling specific lots of jalapenos due to potential Salmonella contamination. Consumers in Louisiana and Texas should check their bags for the listed lot codes.
Whole Foods Market is recalling Pomegranate Guacamole Dip because it may contain jalapenos contaminated with Salmonella. The product was sold in 13 states.
Publix Super Markets is recalling Organic Whole Blueberries due to potential E. coli O145:H28 contamination. Consumers should check expiration dates and discard affected products.
Get Fresh Produce is recalling jalapeno peppers due to potential Salmonella contamination. The product was distributed in Illinois, Indiana, Michigan, and Wisconsin.
Whole Foods Market is recalling Heirloom Tomato Salsa because it was made with jalapenos that may be contaminated with Salmonella.
Publix Super Markets is recalling 37,260 units of Organic Whole Blueberries due to potential E. coli O145:H28 contamination. The product was distributed in eight southeastern states.
Whole Foods Market is recalling Medium Pico de Gallo Guacamole Dip because it may contain jalapenos contaminated with Salmonella.
Whole Foods Market is recalling Mango Pineapple Salsa used in Caribbean Turkey Burgers because the jalapenos may be contaminated with Salmonella.
Whole Foods Market is recalling Spicy Guacamole Dip No Tomatoes because the jalapeños used may be contaminated with Salmonella. The product was sold in 13 states.
Publix Super Markets is recalling Organic Whole Mixed Berries due to potential E. coli O145:H28 contamination. Consumers should check expiration dates and return affected products.
Whole Foods Market is recalling Spicy Guacamole Dip because the jalapenos used may be contaminated with Salmonella.
Whole Foods Market is recalling Mild Guacamole Dip No Tomatoes because it may contain jalapenos contaminated with Salmonella.
Whole Foods Market is recalling Roasted Corn Guacamole Dip because it was made with jalapenos that may be contaminated with Salmonella.
Fresenius Kabi is recalling 625,500 Morphine Sulfate syringes because some were mislabeled and contained Dilaudid instead.
American Regent, Inc. is recalling Selenious Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Tobii Dynavox is recalling TD Navio Maxi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.
American Regent, Inc. is recalling Atropine Sulfate injection vials because they contain particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Nitroglycerin injection vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Tobii Dynavox is recalling TD Navio Midi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.
Grand Central Bakery is recalling specific potato sourdough bread products sold in Washington due to a potential foreign object hazard involving metal pieces.
Medtronic is recalling seven MiniMed 670G insulin pumps because chemical cleaning may have damaged the devices, risking incorrect insulin delivery.
American Regent, Inc. is recalling Aminocaproic Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Shilpa Medicare is recalling 18,434 vials of PEMRYDI RTU (pemetrexed injection) due to reports of green to dark green discoloration in the solution.
American Regent, Inc. is recalling 43,460 vials of Nicardipine Hydrochloride Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent is recalling Multrys (Trace Elements Injection 4) vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Shanghai Ravioli Corporation is recalling approximately 24,900 pounds of frozen, not ready-to-eat Buffalo chicken products produced without federal inspection.
Siemens Healthcare Diagnostics is recalling specific lots of the Emit 2000 Quinidine Assay because unacceptable precision may cause falsely high results, risking improper patient treatment.
American Regent, Inc. is recalling specific lots of Acetylcysteine Solution, USP, 10% due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Acetylcysteine Solution USP due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Regeneron is recalling 21,353 vials of Libtayo (cemiplimab-rwlc) injection nationwide due to a lack of assurance of sterility.
American Regent, Inc. is recalling Cyanocobalamin injections because they contain particulate matter, including hair, glass, and paraformaldehyde.
American Regent is recalling 323,000 vials of Tralement (trace elements injection 4) due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Siemens is recalling 20 units of the Syva EMIT 2000 Quinidine Assay due to precision issues that may cause inaccurate test results.
Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection System Plus catheters due to a potential for arterial sheath tip separation during use.
Gifford's Dairy is recalling specific lots of HomeMaine Power Play Fudge ice cream due to potential rubber contamination.
Siemens Healthineers is recalling Immulite 2000 Syphilis Screen assays because a negative patient bias may cause low reactive results to be reported as nonreactive.
Paragonix Technologies is recalling 1,445 KidneyVault Portable Renal Perfusion Systems because a firmware defect may cause the device to lose configuration, resulting in a blank screen and loss of displayed preservation parameters.
Maquet Critical Care AB is recalling nine Y Sensor Modules for the SERVO-U/-N ventilator systems because they did not undergo required electrical safety and functional tests during production.
Beckman Coulter is recalling DxC 500 AU Clinical Analyzer Modules due to a software defect that may cause erroneous patient test results.
Nutrient Foods, LLC is recalling 16 kits of Protein Cereal Cocoa Crunch because soy was not declared in the contains statement.
Medtronic is recalling 257 MiniMed 780G insulin pumps distributed in Europe because chemical cleaning agents may have damaged the devices, risking incorrect insulin delivery.
Intersurgical Inc is recalling 1,575 One-Piece Guedel Airway devices because they could potentially be occluded or partially occluded.
restor3d Inc. is recalling 59 Veritas Standard Glenoid Baseplates because incorrect machining of peripheral screw holes may cause improper screw engagement.
Siemens Healthineers is recalling 24 units of the Immulite 2000 Syphilis Screen assay due to a potential negative patient bias that may report low reactive results as nonreactive.
Philips is recalling 796 Cardiac Workstation 5000 units worldwide because they may intermittently provide inaccurate native heart rate data.
Lidl US is recalling Vitasia Asian Style Wok Spice Mix because a positive test result detected Salmonella in the product.
Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules due to a software defect that may cause erroneous patient test results.
Fort Defiance Industries is recalling Automated Field Steam Sterilizers because a water recovery system connector may lose ground continuity, creating an unreliable fault current return path.
Medicom is recalling specific lots of Ritmed Neurological Sponges Non-Sterile due to potential unexpected variability in endotoxin levels.
Medicom is recalling specific lots of Ritmed Neurological Sponges Non-Sterile due to potential unexpected variability in endotoxin levels.
AVID Medical, Inc. is recalling 40 packs of Halyard LAVH PACK kits because a component was improperly sterilized, potentially causing leaks.
Bell Sports is recalling specific Pit Boss helmets that may lack proper impact protection, increasing injury risk in crashes.
Gentherm Medical is recalling 46 Innercool Coolblue Console units because overheating of the 115V CPU board may cause the device to shut down.
Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection Systems due to a potential for arterial sheath tip separation or partial tip separation during use.
Bard Access Systems is recalling BD Needle Kits for Powered Drivers because the obturator may lock to the hub, potentially delaying emergency therapy.
Intersurgical Inc is recalling 21,269 One-Piece Guedel Airway devices because they may be occluded or partially occluded. The devices were distributed in six US states.
Philips is recalling 1,810 Cardiac Workstation 7000 units because they may intermittently provide inaccurate native heart rate data.
Sun Pharmaceutical Industries is recalling 1,968 bottles of Carbamazepine 200mg tablets due to CGMP deviations and black spots found on tablets.
Medtronic is recalling 16 MiniMed 640G insulin pumps distributed in Europe because chemical cleaning may have damaged the devices, risking incorrect insulin delivery.
ConvaTec is recalling Esteem Body Soft Convex Urostomy Pouches because they may leak from the cap during use.
Boston Scientific is recalling OverStitch Suture Cinch devices because they may fail to deploy the implant or cut the suture as intended.
Gentherm Medical is recalling 9,714 Blanketrol III thermal regulating systems because overheating of the 115V CPU board may cause the device to shut down.
SDI Limited is recalling 1,444 Dentsply Sirona Capsule Mixers due to a potential for electrical discharge when the unit is unplugged.
Arrowhead DE LLC is recalling 4,171 Arrow-LOK Implants because they did not undergo a required gamma radiation dose audit, which could reduce sterility assurance and lead to patient infection.
Boston Scientific is recalling Suture Cinch Long endoscopic tissue approximation devices because they may fail to deploy the implant or cut the suture.
Spectral Instruments Inc is recalling 40 Lago X units because the 'X-Ray On' banner may briefly disappear during the run readiness check.
Prospector Popcorn is recalling Fudge Brownie Gourmet Popcorn because the packaging incorrectly lists higher amounts of potassium and calcium than the product actually contains.
Mylan Pharmaceuticals is recalling Acamprosate Calcium tablets that failed to meet dissolution specifications.
Kico Knee Innovation is recalling 78 ARVIS Surgical Navigation System Gen 2 units because an internal sensor issue may cause the eyepiece image to appear tilted.
FDA is recalling 327 EndoFLIP Systems because a software error incorrectly flags catheters as expired, making them unavailable for clinical procedures.
Gentherm Medical is recalling 182 Blanketrol II Model 222S thermal regulating systems because overheating of the 115V CPU board may cause the device to shut down.
Paragon 28, Inc. is recalling a custom-made foot implant due to elevated oxygen levels that may reduce material ductility.
Golden State Medical Supply is recalling 1,200 bottles of Carbamazepine 200mg tablets due to tablets containing black specks.
Foundation Medicine is recalling 32 Hamilton Microlab STAR Liquid Handler units due to a software issue causing spontaneous closures.
Spectral Instruments Inc is recalling 35 Ami HTX units because the 'X-Ray On' banner may briefly disappear during the run readiness check.
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