Archive
787 recalls were announced in July 2023.
Of the 787 recalls this month scored against our rubric, 8% are Critical, 46% are Severe.
Which agencies issued them
Kia is recalling 2017–2022 Niro and Niro Plug-in Hybrid vehicles because fluid may leak into the hydraulic clutch actuator, causing an engine compartment fire.
Autocar is recalling 54 model-year 2023 Xpeditor vehicles because damaged fuel filter hoses may leak or disconnect, increasing the risk of engine stall or fire.
Tiffin is recalling 2023 Phaeton motorhomes because damaged fuel filter hoses may leak or disconnect, increasing the risk of engine stall or fire.
Kia America is recalling certain 2023 Sportage vehicles due to a defective electric oil pump controller that may overheat and cause a vehicle fire. Dealers will inspect and replace the controller free of charge.
Farber Specialty Vehicles is recalling one 2021 Ford Transit van because a fuel hose may leak gasoline, increasing the risk of fire.
Rosenbauer America is recalling specific fire trucks because water can enter the winch remote, causing corrosion that may allow the winch to operate unintentionally.
Midway Specialty Vehicles is recalling 2022 Ford Transit vans with Cummins Onan generators because a fuel hose may leak gasoline, increasing fire risk.
Chinook is recalling 2020-2024 Bayside motorhomes because a fuel hose may leak gasoline, increasing the risk of fire.
Temp-Air is recalling 2020-2022 EBB-60 trailers because the trailer tongues may deform and bend, potentially causing instability and loss of control.
Mack Trucks is recalling 2024 LR garbage trucks because missing floor welds may reduce strength, potentially allowing the passenger seat pedestal to buckle in a crash.
Summit Bodyworks is recalling 2019-2022 Ford Transit 350 vehicles with specific generator sets because a fuel hose may not be secured, posing a fire risk.
Airstream is recalling 2019-2023 Ford Transit, 2020 RAM, and 2020-2022 Sprinter recreational vehicles upfitted by Creative Mobile Interiors because a fuel hose may leak gasoline, increasing fire risk.
General Motors is recalling 2013 Buick Verano, Chevrolet Camaro, Sonic, and Volt vehicles because the driver-side air bag inflator may explode during deployment.
Kingsland Food Processing Corp. is recalling various frozen meat and poultry products produced without federal inspection. No adverse reactions have been reported.
Software versions 2.0.64 and older in 2022–2023 Lucid Air vehicles may not respond properly to inverter failures, causing sudden loss of drive power without warning. This increases the risk of crashes.
Soft Play is recalling about 3,500 Sky Wheels play components because the wheels can detach from the overhead rail, causing a fall hazard and risk of injury to children. The company has received 15 reports of detachment, including three reported injuries involving scalp lacerations.
Altec is recalling certain 2022-2023 Digger Derricks and Aerial Devices due to missing circuit breakers on AC power inverters, which could cause electrical fires. Altec will install the circuit breaker free of charge.
Airstream is recalling certain 2023-2024 travel trailers because the SmartPlug 30-amp inlet D-rings may crack when over-tightened, risking electrical arcing and fire.
Jaguar is recalling 2021-2022 I-Pace vehicles due to a faulty high voltage coolant heater that fails to defrost the windshield. This can reduce driver visibility and increase crash risk.
GAF Energy is recalling about 2,100 Timberline Solar Energy Shingles (TLS-1) due to electrical component malfunction that poses a fire hazard. One fire and five thermal incidents resulting in property damage have been reported, with no injuries.
The 2022-2023 Lucid Air may have loose windshield wiper arm nuts, causing the wipers to fail and reducing visibility. No injuries have been reported.
Lucid is recalling 2022-2023 Air vehicles where the rearview camera may fail to display in reverse, violating safety standards. A free over-the-air software update will fix the issue.
Honda CR-V vehicles from 2017, 2020, and 2022 are being recalled for an incorrect driver's door label with wrong tire size and weight ratings. Incorrect tire information may cause premature wear or tire blowout, increasing crash risk.
Certain 2024 Porsche Cayenne models may fail to illuminate rear hazard warning and parking lights when activated shortly after engine shutdown. This defect reduces vehicle visibility and increases crash risk.
Hyundai is recalling 2023-2024 Palisade and Tucson vehicles, plus 2023 Sonata, Elantra, and Kona models for defective oil pump controllers that may overheat and increase fire risk. Owners should park outside until repairs are complete.
True Fitness is recalling about 600 Showrunner II Consoles sold with fitness equipment due to a fire hazard from an exposed wireless charging board. One fire has been reported with no injuries.
SunOpta Grains and Foods Inc. is recalling frozen cherries sold under Great Value, Good & Gather, and Best Choice brands nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Olympus is recalling 17,609 bronchovideoscope units nationwide due to complaints of endobronchial combustion during therapeutic laser procedures, which poses a fire and burn risk to patients.
365 Whole Foods Market Organic Tropical Fruit Medley is recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume this product.
Olympus is recalling OES Bronchofiberscope models due to reports of combustion during laser procedures. This poses a serious burn injury risk to patients.
Target's Good & Gather frozen blueberries are being recalled nationwide due to potential Listeria monocytogenes contamination affecting approximately 3,894 cases.
Olympus bronchoscopes (Models BF-PE2 and BF-TE2) are recalled due to reports of combustion inside the airway during laser-assisted medical procedures. This is an FDA Class I recall.
Good & Gather Triple Berry Blend, sold at Target, is being recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected product.
Trader Joe's Organic Tropical Fruit Blend is recalled due to potential contamination with Listeria monocytogenes from pineapple ingredients. The 16 oz. bags were distributed nationwide.
Target's Good & Gather Mango Strawberry Blend is being recalled nationwide due to potential Listeria monocytogenes contamination. Listeria can cause serious illness.
SunOpta Grains and Foods is recalling Good & Gather Organic frozen cherries and berries distributed nationwide by Target due to potential Listeria monocytogenes contamination.
Townsend Farms' Private Selection frozen blueberries, strawberries, and mangoes are recalled due to potential Listeria monocytogenes contamination. Approximately 34,944 bags were distributed across 16 U.S. states.
Abiomed's Impella CP cardiac pump can be damaged by interaction with replacement heart valves, potentially causing blood clots. The FDA classified this as a Class I recall of 9,252 units worldwide.
Abiomed is recalling Impella CP with SmartAssist blood pumps due to risk of motor housing interaction with transcatheter aortic valve replacement devices, which can damage the pump's impeller blades and reduce blood flow.
Townsend Farms Inc is recalling Private Selection frozen tropical mango chunks due to potential Listeria monocytogenes contamination. The product was distributed across 16 U.S. states.
Olympus is recalling 9 bronchoscopes (Models BF-P150 and BF-1T150) due to complaints of endobronchial combustion during therapeutic laser procedures. The defect could cause fire and serious burn injuries.
Whole Foods Market is recalling 365 brand organic blackberries due to potential Listeria monocytogenes contamination. The frozen fruit was distributed nationwide.
Aldi's Seasons Choice Mixed Fruit is being recalled nationwide due to potential contamination with Listeria monocytogenes. Affected lot codes are FMX227603, FMX227604, and FMX227605.
Abiomed is recalling the Impella 5.5 with SmartAssist pump due to a risk of impeller blade destruction when used with aortic valve replacement devices. Damage can result in low blood flow and systemic embolization, where broken pump pieces may enter the bloodstream.
Datascope has recalled Cardiosave Hybrid IABP models due to tantalum capacitor failures that may cause unexpected device shutdown, interrupting life-critical cardiac therapy.
Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to capacitor failures that may cause unexpected device shutdown. The devices may stop delivering therapy without warning.
The FDA recalls 284 Olympus EVIS EXERA bronchoscopes due to complaints of combustion during therapeutic laser procedures. Users should stop using affected models immediately.
Impella 2.5 intravascular blood pumps may experience unintended interaction with aortic valve replacement stents, damaging impeller blades and reducing blood flow. Fragments may circulate through the bloodstream.
Scenic Fruit Company recalls Cadia and Trader Joe's frozen pineapple products due to potential Listeria monocytogenes contamination. Consumers should not consume the recalled items.
Olympus is recalling EVIS EXERA III Bronchovideoscopes nationwide due to complaints of endobronchial combustion during therapeutic laser procedures. This FDA Class I recall affects approximately 9,684 units.
The Cardiosave Hybrid Intra-Aortic Balloon Pump may lose the ability to charge batteries in one or both bay slots, potentially interrupting critical therapy if disconnected from AC power. Low battery alarms may alert users before therapy is interrupted.
E B Express Provisions is recalling approximately 622 pounds of canned pork and beef bean stew imported from Brazil because the source establishment is not eligible to export meat to the U.S.
SunOpta Grains and Foods Inc. is recalling nationwide frozen pineapple chunks sold under the 365 Whole Foods Market and Bulk Organic brands due to potential Listeria monocytogenes contamination.
Abiomed recalls Impella LD blood pumps due to potential interaction with aortic valve replacement devices that can damage the pump impeller and cause blood clots. Patients with these devices should contact their healthcare provider.
SunOpta's frozen mango chunks sold nationwide under Great Value and Good & Gather brands are recalled due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Abiomed's Impella 5.0 intravascular blood pump is recalled due to risk of impeller blade destruction when interacting with heart valve replacements. The damaged pump can cause reduced blood flow and potentially release fractured material into the bloodstream.
SunOpta Grains and Foods Inc. is recalling 365 Whole Foods Market Organic Whole Strawberries due to potential Listeria monocytogenes contamination. The frozen strawberries were distributed nationwide.
Walmart's Great Value Mixed Fruit is recalled for potential Listeria monocytogenes contamination. The FDA issued a Class I recall affecting approximately 70,360 cases distributed nationwide.
Frito-Lay is recalling Tostitos Avocado Salsa Jar Dip (15 oz, UPC 2840005597) because certain jars contain undeclared milk allergen. Approximately 100,980 jars were distributed in all 50 states with best-by dates of 2 NOV 23 or 3 NOV 23.
SunOpta Grains and Foods Inc. is recalling 365 Whole Foods Market Organic Sliced Strawberries & Bananas due to potential Listeria monocytogenes contamination. The frozen fruit products were distributed nationwide.
Braga Fresh Foods is recalling 673 cases of 365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits due to undeclared milk and egg allergens. Consumers with allergies to these allergens should not consume these products.
SunOpta's Good & Gather brand frozen mixed fruit blend is recalled nationwide due to potential Listeria monocytogenes contamination. Affected consumers should not consume this product and should return it to the retailer.
Olympus BRONCHOVIDEOSCOPE Model BF-Q170 is recalled nationally due to complaints of endobronchial combustion during therapeutic laser procedures, classified as FDA Class I.
Aldi's Seasons Choice frozen tropical fruit blend is being recalled due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Townsend Farms is recalling Private Selection 48oz Classic Fruit Medley due to potential contamination with Listeria monocytogenes. The frozen product was distributed across 16 states.
Rose Street Bread Lab is recalling 27 loaves of Rose Street Patisserie Multi Grain Bread due to undeclared sesame. Consumers with sesame allergies risk serious allergic reactions.
The Cardiosave Rescue Intra-Aortic Balloon Pump may lose battery charging ability in one or both bays, potentially interrupting therapy if disconnected from power. Low battery alarms may alert users before therapy stops.
Medline is recalling probe cover kits with ultrasound gel due to inadequate barriers at the seams that may compromise sterility during diagnostic ultrasound procedures.
Kenai Red Fish Company is recalling Frozen Wild Alaska Smoked Salmon Spread due to incomplete allergen labeling. The label does not properly declare the presence of salmon and anchovies, major fish allergens that could affect consumers with fish allergies.
Central America Products Corporation is recalling Soft Cream Spread (16oz bags, lot code 0725/23) distributed in Florida due to undeclared milk. The product was not properly labeled for milk content, posing a risk to consumers with milk allergies.
Materialise N.V. is recalling MRI Biomet Pin Guides for total knee arthroplasty because the wrong patient-specific device was included in a shipment. Using an incompatible guide could affect surgical planning and implant placement.
C&E Farms is recalling 2,580 mini-bins of bulk romaine lettuce distributed to Massachusetts and Minnesota due to possible contamination with deer droppings. Consumers should not consume the recalled product.
TigerTough is recalling specific seat covers because stitching may prevent the side air bag from deploying correctly in a crash.
Baxter Healthcare is recalling the GEM FLOW COUPLER Monitor due to an LCD display error that may fail to indicate the correct active channel when powered on using battery power. This could lead to incorrect channel selection during use.
DiaSorin Molecular is recalling the Simplexa Direct Amplification Disc Kit due to potential malfunction that could cause liquid to spill from the device.
FDA recalls RET Distal Probe due to manufacturing defect where DNA sequences used in production were inverted. The defect affects 61 units distributed in California, Florida, Ohio, and South Carolina and may impact diagnostic accuracy.
Medline Industries is recalling approximately 23,938 units of sterile ultrasound probe cover kits distributed worldwide from December 2017 to May 2023 due to inadequate barriers at seams that could compromise sterility during diagnostic ultrasound procedures.
Advanced Compounding Solutions is recalling 493 syringes of succinylcholine chloride injection due to potential contamination from manufacturing facility violations affecting product sterility.
New England Life Care is recalling Vancomycin HCl IV bags due to potential CGMP violations that may have compromised the production environment. The recall affects 209 bags distributed nationwide.
Medline is recalling 10,080 ultrasound probe cover kits because the seams may not seal properly, potentially compromising barrier protection. The kits were distributed worldwide from December 2017 through May 2023.
Fry Daddy's Gluten Free Super Ranch Jalapeno Party Mix is being recalled because it contains undeclared walnut. Consumers with walnut allergies should not consume the product.
Botanas Michoacanas is recalling Churritos Corn Flour sticks due to undisclosed sesame in the product label. Sesame is present in the ingredient list but not disclosed in the Contains statement.
Medline is recalling 173,449 sterile probe cover kits due to inadequate seam barriers that may compromise sterility. The affected units were distributed worldwide between December 2017 and May 2023.
Medline Industries is recalling ultrasound probe cover kits used in invasive procedure trays due to inadequate seam barriers that may allow contamination. The recall affects 11,413 units distributed worldwide between December 2017 and May 2023.
Medline Probe Cover Kits may have inadequate seam barriers that could allow contamination during diagnostic ultrasound procedures. Approximately 575 units have been distributed worldwide since December 2017.
Medline Industries is recalling ultrasound probe cover kits due to inadequate barriers at the seams. The defect may allow contaminants to reach the patient during diagnostic ultrasound procedures.
The UFSK Treatment chair 500 XLE's electrical seat drive may wear unexpectedly, causing the chair to fail to hold position while the patient is seated in an inclined position. Healthcare facilities should contact the manufacturer regarding affected units.
SterRx recalled 2,088 bags of Norepinephrine 32 mg per 250 mL (Lot #490100) distributed nationwide due to lack of sterility assurance. The recall affects a critical care medication used in intensive care settings.
Medline is recalling 770,147 ultrasound probe cover kits worldwide due to inadequate barriers at the seams. The defect could allow contamination during diagnostic ultrasound procedures.
Medline Probe Cover Kits used in diagnostic ultrasound procedures are recalled because probe covers may have an inadequate barrier at the seams, potentially allowing contamination.
Medline Probe Cover Kits used during ultrasound procedures may have an inadequate barrier at the seams that could compromise sterility. The manufacturer is recalling 180 units distributed worldwide between December 2017 and May 2023.
Medline is recalling Probe Cover Kits (model DYNJ60126B) with an inadequate barrier at the seams that may compromise sterile protection during ultrasound procedures. The kits were distributed worldwide between December 2017 and May 2023.
Medline Industries is recalling ultrasound probe cover kits with inadequate barriers at the seams that could allow contamination during procedures. Approximately 3.7 million units distributed worldwide between December 2017 and May 2023 are affected.
Fry Daddy's Jalapeno Party Mix is recalled due to undeclared walnut allergen. Affected bags were sold in Michigan with sell-by dates from June 1 to December 31, 2023.
Medline is recalling 4,398 probe cover kits used in ultrasound procedures due to inadequate seam barriers that may compromise sterility. The kits were distributed worldwide from December 2017 through May 2023.
Medline is recalling 4,644 sterile ultrasound gel probe cover kits with potentially inadequate seams that could compromise barrier integrity during ultrasound procedures.
Medline is recalling 2,304 probe cover kits because the seams may not provide adequate barrier protection during ultrasound procedures. Affected kits were distributed worldwide from December 2017 to May 2023.
Fry Daddy's Brand recalls Gluten Free Cheddar Party Mix 10oz bags due to undeclared walnut, a major allergen. The recall affects 1,624 retail units distributed in Michigan.
Medline is recalling Probe Cover Kits (Models CVI4325 and DT13351A) distributed worldwide from December 2017 to May 2023. The probe covers may have inadequate barrier protection at the seams, posing a contamination risk during diagnostic ultrasound procedures.
Medline is recalling ultrasound probe cover kits containing sterile ultrasound gel due to an inadequate seam barrier. The defect may compromise sterility during diagnostic ultrasound procedures.
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