Archive
693 recalls were announced in August 2023.
Of the 693 recalls this month scored against our rubric, 2% are Critical, 13% are Severe.
Which agencies issued them
Hyundai is recalling certain 2021-2023 Elantra HEV vehicles due to a software error in the motor control unit that may cause unintended acceleration after releasing the brake pedal, increasing crash risk.
Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds are being recalled due to spindle spacing that can trap a child's torso while preventing their head from passing through, creating a strangulation hazard. At least two children have become entrapped.
Costco is recalling approximately 350,000 Ubio Labs power banks (model PWB1071) that can overheat and ignite. The company has received three fire reports, including one on a commercial flight with four smoke inhalation reports and one minor burn injury.
Honda is recalling certain 2023 Accord Hybrid and CR-V Hybrid vehicles because the electronic continuously variable transmission (e-CVT) may have been improperly manufactured, potentially resulting in loss of drive power and increased crash risk.
Navistar recalls certain 2023 International HV and MV vehicles; driveshafts may break under certain conditions, causing loss of drive power and increasing crash risk. Replacement is free.
Grand Design is recalling 2022–2024 Momentum travel trailers due to underrated safety chains that may not support the trailer's weight. The defect could allow the trailer to detach from the tow vehicle.
Simplay3 Toddler Towers can tip over during use, posing fall and injury hazards to young children. The manufacturer has received 16 reports of tipping, including 10 reports of injuries.
Midwest Lubricants is recalling about 3,000 units of Sodium Hydroxide (Caustic Soda Beads) because the packaging is not child-resistant and the label lacks required hazard information. The product poses a risk of chemical burns and eye irritation.
Saffron Inc. is recalling burger buns because labels fail to disclose wheat and sesame allergens present in the product. The affected products were distributed to one distributor in South Carolina.
ONO LLC is recalling ONO Vegan Blueberry Muffin Protein Overnight Oats because they contain undeclared milk, a common allergen. The product was distributed nationwide and poses a risk to consumers with milk allergies.
A Corsican sheep's milk cheese has been recalled due to possible Listeria monocytogenes contamination. The product was distributed to a customer in Oregon.
Gree is recalling approximately 1.56 million dehumidifiers sold under brand names including GE, Kenmore, SoleusAir, Seabreeze, and Norpole because they can overheat, smoke, and catch fire, creating fire and burn hazards.
Member's Mark Breaded Mozzarella Sticks are being recalled because they contain undeclared egg and soy allergens. Consumers with allergies to these ingredients should not consume the product.
Cava Spicy Hummus (8oz, UPC 89832800227) is being recalled because it contains undeclared sesame. The product was distributed nationwide; consumers with sesame allergies may be at risk.
Betty Lou's Paleo Java Nuts About Energy Balls are being recalled due to undeclared sesame in the product. The recall affects packages distributed nationwide.
Vans gluten-free original waffles are being recalled because they contain undeclared wheat. Consumers with wheat allergies should not consume this product.
Sweet Alchemy Cookies and Cream ice cream in cups and pints distributed in Washington is recalled for not declaring egg, milk, and wheat allergens on the label.
Sweet Alchemy Ice Creamery is recalling Sweet Alchemy Vegan Monkey Berry Bash ice cream distributed in Washington due to undeclared coconut allergen on labels. Affected pints have expiration dates from July 30 to August 21, 2023.
Bellingham Pasta Co is recalling Semolina Spaghetti due to a labeling error: the product contains wheat (as semolina flour) but the label does not declare wheat as an allergen. Wheat-allergic consumers are at risk.
Bellingham Pasta Co. is recalling 38 packages of Semolina Spinach Fettuccine sold in Washington because the label does not declare wheat, a major allergen present in the product.
Bellingham Pasta Co is recalling Semolina Shells due to undeclared wheat. The product label does not declare wheat, posing a risk to consumers with wheat allergies.
Fresh Creative Foods Caesar Salad Kit is being recalled due to potential contamination with deer feces. The recall affects 1,210 cases distributed to one facility in Illinois.
Olympus revised OER-Pro labeling because two endoscope models (LF-V, LF-P) are no longer compatible. Sterilization parameters and cleaning procedures have also changed.
Olympus is revising labeling for the VISERA Tracheal Intubation Videoscope to correct equipment compatibility information and update sterilization procedures. The device is no longer compatible with OER-Pro, OER-Elite, and OER-Mini reprocessors; sterilization and cleaning procedures have changed significantly.
Sweet Alchemy UW Honey ice cream pints distributed in Washington have labels that fail to declare the presence of Egg and Milk allergens. Consumers with allergies to these ingredients should not consume this product.
Bellingham Pasta Co is recalling Semolina Pappardelle pasta because the label declares semolina flour but fails to declare wheat, a common allergen. The recall affects 199 packages distributed in Washington state.
Waldemar Link is recalling LINK MP Monoblock Hip Stem trial instruments because they may require increased force to remove after impaction, potentially prolonging surgery or requiring procedural modification.
LINK MP Monoblock Hip Stem trial instruments may require increased force to remove after impaction, potentially prolonging surgery for affected patients.
Waldemar Link is recalling LINK MP Monoblock Hip Stem trial instruments due to increased force required for removal during surgery, which may prolong the procedure or require modification.
Waldemar Link GmbH recalled LINK MP Monoblock hip stem trial instruments (Size 23) nationwide due to increased force required for removal post-impaction, potentially prolonging surgery time.
Olympus is updating labeling for 686 LF-P fiberscopes to clarify they are no longer compatible with OER reprocessors and specify new 100% ETO sterilization protocol.
Bellingham Pasta Co is recalling Semolina Vegan Rigatoni due to undeclared wheat allergen in the semolina flour ingredient.
Bellingham Pasta Co is recalling 190 packages of Semolina Lemon Black Pepper Linguine because the label declares semolina flour but fails to declare wheat as an ingredient, posing a risk to consumers with wheat allergies.
Sweet Alchemy Strawberry Rhubarb Crisp ice cream sold in Washington has been recalled because its labels do not declare the presence of milk, egg, and wheat allergens.
Sweet Alchemy Vanilla Cubed ice cream sold in Washington was recalled because labels do not declare ingredients, including the allergens Egg and Milk.
Sweet Alchemy Strawberry ice cream in pints fails to declare Egg and Milk allergens on labels. Fifteen pints distributed in Washington are affected.
Ortho-Clinical Diagnostics is recalling VITROS Troponin I ES Calibrators because reagent packs may contain incorrect wells that could produce false negative results. The recall affects 4,013 units distributed worldwide.
Olympus is revising labeling for its OER-Elite, OER-Pro, and OER-Mini endoscope reprocessors due to incompatible endoscope models and incorrect sterilization parameters in previous labeling. The revisions remove two endoscope models from the compatibility list and correct gas sterilization concentration requirements.
Philips Ingenia Elition S MR systems can be circumvented by power cycling to bypass the smoke detection safety interlock that locks after smoke is detected. This could allow continued operation despite fire hazards.
LINK MP Monoblock hip stem trial instruments may require excessive force to remove after impaction, potentially prolonging surgery or requiring procedural modification.
The LINK MP Monoblock hip stem trial instruments may require increased force to remove after implantation, potentially prolonging surgery or requiring modification of the surgical procedure.
Sweet Alchemy Ice Creamery is recalling Lemon Custard ice cream cups because labels fail to declare ingredients, including the allergens Egg and Milk.
Bellingham Pasta Co recalls 168 packages of mixed flavors pasta in Washington due to undeclared wheat allergen in semolina flour. Consumers with wheat allergies may experience allergic reactions.
Siemens has recalled 10 ARTIS angiography systems due to thermal overload hazard in cable connectors. The issue may cause burning smell and loss of imaging functionality, potentially requiring treatment cancellation or system replacement.
Entrans is recalling 2023 Polar Tank SCX9 trailers that may lack a rear impact guard certification plate, failing federal safety standards.
Sweet Alchemy Dough or Die ice cream pints distributed in Washington lack ingredient and allergen declarations on labels. The product contains Egg, Milk, Soy, and Wheat allergens.
Bellingham Pasta Co recalls Semolina Roasted Red Pepper Linguine (14oz) due to undeclared wheat allergen. The product was distributed in Washington state.
Triumph is recalling 2022-2024 Tiger Sport 660 and Trident 660 motorcycles because the MAP hose may become obstructed, causing incorrect engine readings, stalling, and crash risk. Dealers will replace the hose for free.
BMW is recalling 2019-2022 330i, M340i, and other models due to receiver audio module software that may fail to generate proper seat belt warnings, increasing crash injury risk.
C&E Farms is recalling 8,010 mini-bins of bulk romaine lettuce that may be contaminated with deer feces. The affected lettuce was distributed to retailers in seven U.S. states.
FDA recalls Randox RX Series Urea test kits because carryover from prior LDL-cholesterol tests may produce falsely low results, up to 11% below accurate values, potentially delaying diagnosis.
Stryker's HoverMatt 39-inch inflatable transfer mattresses contain 34-inch units inside, reducing available support surface. This increases friction during patient transfers and raises the risk of skin tears.
Siemens recalls ARTIS icono biplane angiography systems with defective cable connectors that may cause thermal overload, burning smell, and loss of imaging functionality during clinical procedures.
Bellingham Pasta Co is recalling Semolina Fettuccine due to missing wheat allergen declaration on labels. Consumers with wheat allergies should not consume this product.
The FDA is recalling 127 Ellacor System devices for a potential bearing adhesive failure in the handpiece. The defect could cause core overlap, leading to prolonged healing and scarring.
LINK MP Monoblock hip stem trial instruments may require increased force to remove during surgery, potentially prolonging procedures or requiring surgical modification.
Philips MR 7700 MRI systems can have their smoke detector interlock safety mechanism bypassed when power cycled after smoke detection, allowing continued operation despite potential fire hazards.
Bellingham Pasta Co. is recalling Semolina Gemelli pasta because the label does not declare wheat, a major allergen, despite wheat being an ingredient. Consumers with wheat allergies should not consume this product.
The UroLift Visual Obturator has an improperly performed weld that may fracture during use, and the welded area can harbor contamination not removed by standard cleaning. Affected units should not be used.
Philips Ingenia Elition X MR systems can have their smoke detection safety interlock bypassed by power cycling the equipment. This vulnerability could allow unsafe operation during hazardous conditions.
Waldemar Link is recalling 24 LINK MP Monoblock Hip Stem trial instruments due to increased force required to remove them after impaction, which may prolong surgery or require procedure modification.
Siemens ARTIS icono floor angiography systems may experience thermal overload in cable connectors during fluoroscopy, causing burning smell and loss of imaging capability. The recall affects 7 units worldwide.
Medline is recalling the Total Hip Kit (REF DYNJ903275S) because the included prep solution expires before the kit itself expires. Sixteen kits with lot code 23CDC733 were distributed nationwide.
Bellingham Pasta Co is recalling semolina linguine due to missing wheat allergen declaration on the label. Consumers with wheat allergies may be at risk.
Eclipse Foods is recalling 14 fl oz Caramel Butter Pecan Cups for the potential presence of ink pen pieces and foreign objects. The affected product was distributed in seven states.
ORTHO-CLINICAL DIAGNOSTICS is recalling VITROS Troponin I ES Reagent Pack due to potential incorrect wells that could generate false negative diagnostic results. Lot 4800 with expiration 10-Jun-2023 is affected.
A trial hip stem implant may require excessive force to remove after insertion during surgery, potentially prolonging the procedure or requiring surgical modification.
Waldemar Link GmbH recalls LINK MP Monoblock hip stem trial instruments due to increased removal force requirements after impaction, which may prolong surgery or require procedural modification.
Sweet Alchemy Toasted Black Sesame ice cream pints lack required allergen labeling for Egg, Milk, and Sesame. Affected products were distributed in Washington.
Sweet Alchemy Blackberry Crumble ice cream pints lack required ingredient and allergen labeling, specifically failing to declare milk, egg, and wheat allergens.
Bellingham Pasta Co is recalling Semolina Bucatini pasta because the label fails to declare wheat, a major allergen present in the product. Consumers with wheat allergies risk allergic reaction.
Sweet Alchemy Strawberry Rhubarb Crumble ice cream distributed in Washington has been recalled because labels do not declare ingredients or allergens including Egg, Milk, and Wheat. Consumers with allergies should not consume this product.
Sweet Alchemy Ice Creamery is recalling 27 pints of its Vegan Nutty for Chocolate ice cream due to missing ingredient and allergen declarations on the label. The product contains peanut and coconut but does not declare these common allergens.
Sweet Alchemy Vegan Lemon Pie ice cream sold in Washington lacks required allergen labeling for coconut and wheat. Consumers with these allergies should not consume this product.
Sweet Alchemy Vegan Raspberry Chip ice cream sold in Washington State lacks allergen declarations for Coconut and Soy on its labels. Allergic consumers should not consume this product.
Bellingham Pasta Co recalls Semolina Sheets because the product contains wheat but the label does not declare it. Affected packages have best-by dates of 7/12, 7/15, or 7/19.
Canon Medical has recalled 12 INFX-8000C tableside consoles due to a printed circuit board that may require replacement. Though procedures may be delayed, x-ray operations can continue using alternative controls.
Olympus revised labeling for the OER-Mini endoscope reprocessor. The company removed LF-V and LF-P endoscopes from the list of compatible devices and updated sterilization procedures.
Medtronic is recalling Solera Awl Tip Tap surgical devices due to incorrect laser marking. Thirteen devices were distributed in Florida, Colorado, Indiana, South Carolina, Texas, and Utah.
Philips is recalling 601 Ingenia Elition X MR systems because a diagnostic cable may not have been properly installed, though system operation is not affected.
Philips Ingenia Elition S MR systems may have an improperly installed cable connecting the SmokeDetector Interlock to the host PC. This affects service diagnostics only and does not impact system functionality.
B. Braun Medical Inc. is recalling 43,812 bags of 0.9% Sodium Chloride Injection due to incomplete or missing labeling, including warnings and instructions for use.
Sun Pharmaceutical recalls Dofetilide 500 mcg capsules nationwide due to out-of-specification results in content uniformity testing. Affected lot DNE0217A with expiration 01/2025 may not meet pharmaceutical specifications.
Waldemar Link is recalling LINK MP Monoblock hip stem prosthetics that may require increased force to remove after surgical implantation, potentially prolonging surgery.
Medtronic is recalling InterStim Self-Adhesive Ground Pad (lot 60347246) due to incorrect expiration date labeling. Affected units were distributed internationally including to Iran.
Philips MR 7700 Magnetic Resonance systems may have an improperly installed diagnostic cable. The cable does not impact system functionality or patient safety.
LINK MP Monoblock hip stem trial instruments may require increased force to remove after impaction, potentially prolonging surgery or requiring procedure modification. No injuries or illnesses have been reported.
Bellboy Import Corporation is recalling approximately 551 pounds of frozen, raw pork belly because the products were not presented for import reinspection into the United States.
Indian Motorcycle Company is recalling 2023 Pursuit Limited motorcycles because the fuel line may have been improperly assembled. This can cause engine stall and increase the risk of a crash.
Kia is recalling certain 2023 Sorento vehicles. Air bag warning labels on sun visors may detach, preventing occupants from being warned about air bag deployment risks in a crash.
Nissan North America is recalling 2020-2022 Sentra vehicles because the left or right tie rod may bend, potentially breaking and causing loss of steering control. Owners should contact their dealer for free interim repairs.
Chrysler is recalling certain Jeep Grand Cherokee and Wagoneer models (2021–2024) due to a software issue that may prevent the rearview display from showing when backing up. This violates federal rear-visibility standards.
Certain 2022-2023 Jeep Compass vehicles have a software error that prevents the instrument panel brightness from being adjusted. Drivers may not clearly see critical safety information like speed and warning lights.
Chrysler is recalling specific Mopar Central Vision Park Assist Modules because software may prevent the rearview image from displaying in reverse, increasing crash risk.
Chrysler is recalling specific Mopar Body Control Modules because incorrect software may prevent instrument panel brightness adjustment, potentially obscuring critical safety information.
Trail King is recalling 1992-2023 trailers because shims may detach from pin-on axles, creating a road hazard.
Forest River is recalling 2024 Coachmen Beyond, Galleria, and Nova motorhomes because cracked shore power inlet D-rings may cause electrical arcing and fire.
Mercedes-Benz is recalling 880 2023 vehicles because a software error may prevent the exit warning system from alerting occupants to approaching vehicles.
Certain 2023 Ford F-250, F-350, and F-450 trucks with the Pro Trailer Hitch Assist feature may not display the rearview camera image, reducing rear visibility and increasing the risk of a crash.
Alliance RV is recalling 2023-2024 Paradigm travel trailers because an incorrectly wired breakaway switch may prevent emergency brakes from activating if the trailer detaches.
Looking for a different month? Back to 2023.