Archive
547 recalls were announced in July 2024.
Of the 547 recalls this month scored against our rubric, 2% are Critical, 16% are Severe.
Which agencies issued them
Specialty Manufacturing is recalling 3,853 vehicles because an under-rated fuse in the rearview mirror switch may overheat and cause a fire.
Dongguan Biaoming is recalling JecoEV Tesla to CCS charging adapters sold on Amazon due to missing over-temperature protection and insecure latching, posing fire and electrical shock risks.
Daimler Vans USA is recalling certain 2023-2024 Mercedes-Benz Sprinter vehicles due to rear suspension U-bolts with reduced strength from improper heat-treatment. The defect can cause the rear axle to shift, increasing crash risk.
Prevost recalls certain 2005-2024 buses with wheelchair lifts due to a potentially steep bridging device that can cause wheelchair instability. Affected owners should contact Prevost for a free replacement.
Volvo Bus is recalling 2024 9700 vehicles because improperly tightened nuts on the steering gear link rod may loosen, potentially causing loss of steering control.
Keystone is recalling specific 2024 travel trailers because metal sidewalls may detach during transit, creating a road hazard.
Grand Design is recalling certain 2024 Reflection travel trailers due to missing electrical circuit protection. The wiring may become damaged and short circuit, posing a fire risk.
Mercedes-Benz is recalling 2023 GLC 300 4MATIC vehicles because insufficiently tightened dashboard bolts and loose heater connections may cause airbag deployment issues or fire.
Nova Bus is recalling 2021-2024 LFS buses due to an air leak in the parking brake valve that can cause unexpected parking brake engagement without activating brake lights, increasing crash risk.
Autocar is recalling 841 2023-2024 Xpeditor trucks because a missing retaining ring on the cab tilt hinge pin could cause the pin to separate, creating a road hazard and increasing crash risk.
Nova Bus is recalling certain 2022-2023 LFS buses due to incorrectly aligned windshield wiper arms that can cause wiper blades to collide. Damaged blades reduce visibility and increase crash risk.
Chrysler is recalling 2021-2022 Jeep Cherokee vehicles with improperly secured right-side curtain airbag connectors that may prevent deployment, increasing injury risk in a crash.
Gillig is recalling 2023-2024 Low Floor transit buses because improperly tightened steering spline shaft fasteners may allow the shaft to loosen, increasing crash risk.
Al-Safa US LLC is recalling approximately 2,010 pounds of frozen ready-to-eat chicken products that may be contaminated with Listeria monocytogenes.
Carparts.com is recalling specific MH taillights and headlights that do not illuminate sufficiently, failing to meet federal safety standards and increasing crash risk.
AMB FOODS INC is recalling Pop a Nosh Mixed Munch snacks due to undeclared wheat allergen. Approximately 2,100 units distributed in New York contain wheat, which is not labeled on the product.
The Life2000 Ventilator may fail to charge or experience intermittent charging behavior due to damage to the battery charger dongle. This FDA Class I recall affects approximately 2,510 units distributed nationwide.
Certain 2025 Freightliner and Western Star commercial vehicles may have improperly heat-treated tie rod assemblies that can fail, potentially causing loss of steering control and increasing crash risk.
Andersen & Sons Shelling, Inc. is recalling its macadamia nuts due to Listeria monocytogenes contamination. Approximately 2,850 pounds were distributed in the United States.
Philips is recalling 307 SENSE XL TORSO COIL 3.0T units used in MR imaging systems worldwide due to potential for coils to overheat and cause patient burn injuries.
Inspire Medical Systems recalls the Model 3028 Implantable Pulse Generator due to a manufacturing defect causing electrical leakage and system malfunction that requires revision surgery. The recall affects 24 devices distributed in the US and Germany.
GLOBAL MIX INC. is recalling Tejocote Root Products sold under multiple brand names because they contain Yellow Oleander, a toxic plant. Consumers should not use these products.
ELV Control Herbal Supplement is being recalled because it contains yellow oleander instead of the labeled tejocote ingredient. Yellow oleander is toxic to humans. The product was distributed through authorized dealers and e-commerce platforms.
Pop a Nosh Mixed Munch in Honey BBQ flavor is recalled due to undeclared wheat allergen. Approximately 2,100 units distributed in New York may lack proper allergen labeling.
Philips is recalling SENSE XL TORSO COIL units used in MRI imaging because the coils may heat up excessively and cause patient burns. This FDA Class I recall affects 729 units distributed worldwide.
Queso Chonero Special White Cheese has been recalled due to Listeria monocytogenes contamination. The product was distributed in Illinois.
Philips recalled 14 SENSE XL Torso Coils worldwide due to potential overheating. The coils could heat up during use and cause patient burn injuries.
BMW is recalling 2006-2012 3 Series vehicles because a steering wheel air bag inflator may explode during deployment, posing a risk of serious injury.
Green Life Farms Baby Arugula in 4.5 ounce clamshells has been recalled due to potential Salmonella contamination. The affected product has lot number LW15124 and a sell-by date of 6/15/24, distributed in Florida.
Classic Delight LLC is recalling Wakefield Bacon, Egg & Cheese Bagels (Item 806620) due to possible Listeria monocytogenes contamination. The recall affects 2,663 cases distributed across 14 states.
Classic Delight LLC is recalling 1,626 cases of Wakefield Charbroiled Cheeseburgers due to potential Listeria monocytogenes contamination. The product was distributed to 14 states; consumers should discard affected items.
American Honda Motor is recalling about 40,700 model year 2023-2024 off-road motorcycles (CRF50F, CRF110F, CRF125F) because the handlebar grip can detach, posing a crash and injury hazard. One crash resulting in a knee injury has been reported.
Medtronic is recalling 8 units of the COBALT XT HF CRT-D MRI SureScan implantable cardioverter defibrillator due to manufacturing defects identified during quality control testing.
Medtronic is recalling 11 units of the COBALT XT HF QUAD CRT-D MRI SureScan implantable cardioverter defibrillator due to a manufacturing defect involving weld cracks that failed quality control testing.
Siemens AXIOM MULTIX MP radiographic X-ray tables are being recalled due to a potential short circuit in the touch display's power supply unit that may cause overheating or fire. 12 units nationwide are affected.
Medtronic is recalling eight COBALT XT VR MRI SureScan implantable cardioverter defibrillators due to weld cracks that caused device failure during manufacturing.
Draeger recalls 34,102 Infinity M500 monitoring systems due to electrical safety noncompliance. The devices pose a potential risk of electrical shock, burns, and cardiac arrhythmia.
Medtronic is recalling 36 COBALT DR MRI SureScan implantable cardioverter defibrillators due to a weld crack manufacturing defect. The defect was identified during manufacturing quality checks.
Classic Delight LLC is recalling Wakefield Chorizo & Egg on Ciabatta due to possible Listeria monocytogenes contamination. The product was distributed across 14 states.
Siemens recalls AXIOM MULTIX MT radiographic X-ray tables due to a short circuit in the power supply unit that may cause overheating and fire. 7 units are affected nationwide.
Universal Bakery Organic Aussie Bites are being recalled because they are labeled as gluten-free but testing found gluten content above 20 parts per million. The product was distributed to Washington and Illinois.
Mermaid Medical is recalling 190 D*Clot® HD Rotational Thrombectomy Systems worldwide due to failed sterility testing that indicates the sterility barrier may not be fully intact.
Wakefield Sausage, Egg & Cheese Biscuit (Item 806638) has been recalled in 14 states due to possible Listeria monocytogenes contamination. Affected products have best-by dates from February 2024 through March 2025.
Siemens RAPIDPoint 500e software version 5.3 incorrectly labels capillary blood samples as arterial on laboratory information system displays, potentially leading to misinterpretation of results and diagnostic errors.
Medtronic is recalling five implantable defibrillators due to a manufacturing defect where weld cracks caused devices to fail quality testing. The defective devices were identified during manufacturing and did not reach patients.
CentriMag Primary Console units may completely shut down without alarm during power surges above 1.8kV, requiring emergency switch to backup circulatory support.
Nine Medtronic COBALT DR MRI implantable cardioverter defibrillators are recalled due to a weld crack that caused devices to fail manufacturing quality checks.
Certain GE CARESCAPE patient monitors may fail to power on after mains power loss during battery maintenance, potentially delaying recognition of patient condition changes.
Biomet recalled RingLoc hip acetabular cup components that may have been incorrectly assembled with a mismatched locking ring, potentially causing joint instability. Affected patients may require surgical intervention.
Classic Delight LLC is recalling turkey and cheese sub sandwiches that may be contaminated with Listeria monocytogenes.
Pacira Pharmaceuticals recalls Zilretta intra-articular injectable suspension nationwide after the product failed dissolution specifications in stability testing.
Classic Delight Twin Breaded Chicken Sliders distributed to institutional food service are being recalled due to possible contamination with Listeria monocytogenes. The recall affects 1,767 cases across 14 states.
Pfizer recalls 220,400 cartridges of Labetalol Hydrochloride injection due to potential incomplete crimp seals that could compromise sterility. Affected lots should not be used; healthcare providers should contact Pfizer for guidance.
Tillamook Colby Jack/Monterey Jack Cheese Slices are being recalled due to plastic material found in the cheese. Consumers in Washington and Utah should not consume this product.
Classic Delight LLC is recalling Wakefield Sausage, Egg & Cheese Muffins (Item 806646) distributed across 14 states due to possible Listeria monocytogenes contamination.
Classic Delight LLC recalls Wakefield Sausage & Egg Pancake products (Item 942821) due to possible Listeria monocytogenes contamination. Affected products were distributed across 14 states.
GE CARESCAPE Canvas Smart Display monitors may fail to turn on after a power loss, particularly following battery replacement, potentially delaying recognition of patient condition changes.
Integra LifeSciences is recalling CUSA Excel C2600 surgical handpieces due to potential housing cracks that may delay treatment. The recall affects 2,652 units distributed nationwide and internationally.
Hatch Baby is recalling power adapters sold with Rest 1st Generation sound machines because the plastic housing can detach from the adapter when unplugged, exposing electrical prongs and creating a shock hazard. The firm has received 19 reports of the housing coming off, including two reports of minor electrical shock.
Lidl US TRADING is recalling Chef Select 2 Garlic Baguettes due to undeclared wheat and milk allergens caused by foreign language labeling. Consumers with allergies to wheat or milk should not consume these products.
Siemens is recalling 2 AXIOM Vertix MD imaging systems nationwide due to a potential fire hazard from a short circuit in the power supply unit that may cause overheating.
Roche is recalling Accu-Chek Guide (SC) blood glucose meters that may display readings in mmol/L instead of mg/dL, appearing approximately 18 times lower than actual. This could lead to incorrect treatment decisions and long-term diabetes complications.
Classic Delight LLC recalls Wakefield Ham & Cheddar Pretzel Croissant (1323 cases) due to possible Listeria monocytogenes contamination. Product distributed across 14 states with multiple lot numbers and best-by dates through March 2025.
Chrysler is recalling 2019 Alfa Romeo Stelvio vehicles for a defective seat belt buckle switch sensor that may prevent front airbags from deploying. Dealers will repair the connection at no cost.
Coast Quality Pharmacy is recalling Progesterone 200 mg compounded sublingual tablets nationwide due to discovery of broken metal pieces embedded in tablets. Patients should contact their healthcare provider.
Classic Delight LLC recalls Wakefield Ham, Egg & Cheese Croissants due to possible Listeria monocytogenes contamination. The product was distributed across 14 US states; consumers with affected products should not consume them.
Medtronic is recalling EVERA S VR implantable cardioverter defibrillators due to a potential manufacturing defect involving a weld crack that can cause device failure. The defect was identified during manufacturing leak testing.
Classic Delight LLC is recalling 3,411 cases of Wakefield Charbroiled Cheeseburger Kaiser Roll due to possible Listeria monocytogenes contamination. The product was distributed in 14 states.
Classic Delight LLC is recalling 1,032 cases of Wakefield Pretzel Bacon Angus Cheeseburger due to possible Listeria monocytogenes contamination. The product was distributed across 14 states.
Focusee is recalling about 27,400 Tideway High-Speed Hair Dryers because they lack immersion protection and pose an electrocution or shock hazard if they fall into water while plugged in. Consumers should stop using the product immediately.
FEEL GOOD FOODS INC is recalling Cream Cheese Stuffed Plain Mini Bagels due to undeclared gluten. Consumers with gluten sensitivity or celiac disease should not consume this product.
Classic Delight LLC is recalling Wakefield Bacon Cheeseburger Kaiser Rolls due to possible Listeria monocytogenes contamination. The recall affects 1,079 cases distributed across 14 states.
Medtronic is recalling 82 implantable cardioverter defibrillators due to a manufacturing defect involving weld cracks discovered during quality control testing before distribution to patients.
FEEL GOOD FOODS INC is recalling Cream Cheese Stuffed Everything Mini Bagels nationwide because the product contains gluten not listed on the label. Consumers with gluten sensitivity should not consume this product.
Classic Delight LLC is recalling 16,572 cases of Turkey Sausage & Egg Muffins (Item 73131) distributed across 14 states due to possible Listeria monocytogenes contamination.
Medtronic is recalling 58 COBALT XT HF QUAD implantable cardioverter defibrillators worldwide due to a weld crack manufacturing defect that caused devices to fail quality checks.
Chrysler is recalling certain Alfa Romeo Stelvio and Giulia models with incorrect tire placard information. Incorrect tire pressure or size specifications can lead to under-inflation or wrong tires, increasing crash risk.
Dental EZ Group is recalling certain Titan Scaler Tip (Perio, Model 261669) units due to an oversized tip holder condition that may prevent proper seating, creating a risk of injury during use.
Cook Incorporated is recalling 15 units of the Ultrathane Mac-Loc Locking Loop Multipurpose Drainage Catheter due to incorrect expiration dates on product labels that extend beyond the device's true expiration date. Affected units were distributed to Spain and the Netherlands.
Siemens Medical Solutions is recalling AXIOM MULTIX MP radiographic X-ray tables due to a potential short circuit in the power supply that may cause overheating and fire. The recall includes 20 units with U.S. nationwide distribution.
The James Skinner Co. is recalling Marketside Cinnamon Pecan Braid Danish pastry due to incorrect labeling that fails to declare pecans. Consumers with pecan allergies who consume the product could experience allergic reactions.
Medtronic is recalling 6 units of the MIRRO MRI VR SureScan implantable cardioverter defibrillator due to a potential manufacturing defect. The devices failed manufacturing quality checks because of a weld crack.
Classic Delight LLC is recalling Wakefield Spicy Hawaiian Sliders due to possible contamination with Listeria monocytogenes. The recalled product was distributed across 14 states.
Medtronic is recalling two PRIMO MRI DR SureScan implantable cardioverter defibrillators due to a potential manufacturing defect involving weld cracks detected during manufacturing quality testing.
Siemens is recalling the AXIOM Vertix Solitaire diagnostic imaging component due to a short circuit in the Touch Display's power supply unit that may cause overheating and fire. Two units with serial numbers 1239 and 1241 are affected.
Classic Delight LLC is recalling 384 cases of Classic Delight Turkey & Cheese On Round Bun (Item 6731) due to possible contamination with Listeria monocytogenes. The product was distributed to food service facilities in 14 states.
Medtronic is recalling 40 EVERA MRI S DR SureScan ICDs (Model DDMC3D4) due to manufacturing weld cracks that caused devices to fail leak tests. The defect was identified during manufacturing; no patient harm has been reported.
Medtronic is recalling 14 Cobalt XT HF CDT-D MRI SureScan implantable defibrillators due to a manufacturing weld defect that could cause device failure.
Siemens is recalling AXIOM MULTIX MT X-ray patient tables due to a potential short circuit in the Touch Display power supply that may cause overheating and fire. Fifty units were distributed nationwide.
Medtronic is recalling 14 units of EVERA MRI S VR SureScan implantable cardioverter defibrillators (Model DVMC3D4) due to potential weld cracks discovered during manufacturing. No patient injuries have been reported.
Siemens MULTIX TOP I PRO X-ray tables are recalled due to a power supply short circuit that may cause overheating and fire. Three units have been identified.
Medtronic recalls 13 MIRRO MRI VR SureScan implantable cardioverter defibrillators (ICDs) due to a manufacturing weld crack. The defect was identified and caused device failure during the manufacturing leak check quality control test.
Medtronic is recalling five units of its EVERA MRI S DR SureScan implantable cardioverter defibrillator due to a manufacturing defect—a weld crack that caused failure during quality control testing.
Classic Delight LLC is recalling 1,477 cases of Blazin' Chicken Kaiser Rolls due to possible Listeria monocytogenes contamination. The affected product has been distributed across multiple states.
Medtronic recalls 46 PRIMO MRI VR SureScan implantable cardioverter defibrillators due to a manufacturing defect. Weld cracks identified during manufacturing quality checks could cause device failure.
NovaGuide 2 Traditional Ultrasound systems may have grounding cables that can be inadvertently disconnected during use, creating risk of electrical shock and equipment malfunction. Twenty-eight systems have been distributed nationwide.
GE Healthcare medical monitors may fail to display following a power loss event after CPU battery replacement, potentially delaying patient condition recognition.
Classic Delight Chili Cheese Dogs are being recalled due to possible contamination with Listeria monocytogenes. The recall affects 20,817 cases distributed across 14 states.
Golden State Medical Supply is recalling Duloxetine 30mg capsules nationwide due to contamination with N-nitroso-duloxetine, a nitrosamine impurity above the FDA's proposed safety limit. Affected lots expire January 31, 2025.
Classic Delight LLC is recalling 1,119 cases of Classic Delight Turkey Ham & Cheese Sub (Item 311) distributed across 14 states due to possible Listeria monocytogenes contamination.
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