Archive
412 recalls were announced in July 2021.
Of the 412 recalls this month scored against our rubric, 3% are Critical, 27% are Severe.
Which agencies issued them
Cummins is recalling specific L9 Diesel Engines equipped with remote Stage 2 fuel filters because a fuel leak may occur from the hose between the fuel pump and filter head.
Jayco is recalling certain 2019-2021 recreational vehicles with Hehr 6400 series windows due to adhesive failure. The window vent may detach, increasing the risk of crash or injury.
Summit Bodyworks is recalling one 2017 Freightliner M2-106 because its rear LED lights are too bright, potentially blinding other drivers and increasing crash risk.
Micro Bird is recalling 2003-2022 school buses because the service door emergency release handle may bind, preventing evacuation in an emergency.
Micro Bird is recalling 1,323 transit buses because the service door emergency release handle may bind, preventing evacuation in an emergency.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because an incorrect voltage converter socket may cause excessive voltage in the second-row power outlet, increasing fire risk.
Mercedes-Benz is recalling certain 2020-2021 models because side crash sensor connectors may come loose, delaying airbag and seatbelt activation during side impact crashes. Dealers will inspect and replace sensors at no cost.
Forest River and Coachmen recreational vehicles with Hehr 6400 Series windows are being recalled due to adhesive failure that may cause window vents to detach. Detachment increases the risk of crashes and injuries.
Fuel may leak at a pipe connection in affected 2021-2022 Hyundai Santa Fe and Sonata vehicles with 2.5L engines, increasing fire risk.
Nissan is recalling 2021 Rogue Sport vehicles because liftgate hinges may separate during rear-end crashes, compromising door retention. Dealers will replace the hinges free of charge.
LoHi Tech is recalling about 24,900 SOWTECH Espresso Machines (Model CM6811) because the glass carafe can break during use, posing a burn hazard. The firm has received 48 reports of breaking carafes, resulting in five burn injuries.
BMW is recalling 2018-2019 X3 and X4 vehicles because the front passenger air bag may fail to deploy due to a sensor assembly error.
Chrysler recalls 21,258 model year 2020-2021 Dodge Challenger, Dodge Charger, and Chrysler 300 vehicles for windshields that may not be properly bonded and could detach in a crash. Dealers will replace the windshield urethane sealant free of charge.
Thor Motor Coach is recalling multiple RV models due to defective adhesive bonding in Hehr 6400 series windows. The vented portion may detach, increasing risk of crash or injury.
BMW is recalling one 2019 X5 xDrive 40i because a manufacturing defect in the instrument panel may prevent the passenger air bag from deploying properly in a crash.
Maintainer is recalling 2019-2020 Service/Mechanics Bodies mounted on International MV607 vehicles because crane mounting bolts are too short to securely attach the crane.
Canyon Furniture has recalled about 1,200 Creekside Kids Five-Drawer Chests sold at Rooms To Go because the chests are unstable without wall anchoring and pose tip-over and entrapment hazards to children.
Kia is recalling 2022 K5 vehicles with 2.5L turbocharged engines due to fuel leaks that increase fire risk. Dealers will repair the fuel pipe at no cost.
General Motors is recalling certain 2022 Chevrolet Bolt EV and Bolt EUV vehicles because driver-side air bag fasteners may be missing or improperly tightened. This could prevent the air bag from deploying properly in a crash.
ECHO EGi-2300 Watt Generators can overheat and catch fire, posing a fire and burn hazard. The manufacturer has received four reports of overheating or fire, though no injuries have been reported.
NSNY Distributor Inc is recalling Ginseng Power 5000 capsules nationwide because they contain undeclared sildenafil and/or tadalafil, prescription medications not listed on the label or approved for sale in this product.
Premium OrgaZEN 7000 capsules distributed nationwide have been recalled because they were marketed without FDA approval and contain undeclared sildenafil and/or tadalafil, prescription drugs that pose serious health risks.
Guan's Seafood Mushroom products are being recalled because sampling found Listeria monocytogenes contamination. The affected products were distributed to California, Hawaii, Florida, Illinois, Minnesota, and Arizona.
Altec is recalling 2020-2021 D2000, D3000, and D4000 Derrick diggers because an improperly seated retaining ring allows the boom to rotate unintentionally, increasing injury risk.
Interstate Food Products is recalling Little Hatch's Spicy Queso due to Listeria monocytogenes contamination and undeclared soy lecithin. The product was distributed across multiple states.
Lakeview Farms LLC is recalling Smilin' Bob's All Natural Smoked Fish Dip due to potential Listeria monocytogenes contamination. The recall affects 48 cases distributed to five distributors in Florida.
DiBAR LABS Hand Sanitizer (ethyl alcohol 70%, 8 FL OZ) is being recalled because FDA testing found three lots contain methanol contamination and have ethanol content below the label claim.
Dibar Labs is recalling Advance Hand Sanitizer (70% ethyl alcohol, 16 FL OZ) distributed nationwide because it was manufactured under the same conditions as lots found to contain methanol.
ProtectoRx hand sanitizer (ethyl alcohol 70%) is being recalled nationwide because some lots were found to contain methanol and all lots were manufactured under the same conditions as the contaminated product.
Magellan Diagnostics recalls LeadCare Plus Blood Lead Test Kit after control tests generated low results, potentially underestimating patient blood lead levels. Affected lot numbers include 2011MU, 2104MU, and 2108MU.
The LeadCare II Blood Lead Test Kit may generate artificially low control test results, causing blood lead levels to be underestimated in patient samples. Kits were distributed worldwide.
Interstate Food Products is recalling Little Hatch's Roasted Chili Salsa (Hot, 13.5 oz) because product samples tested positive for Listeria monocytogenes, a potentially harmful bacteria.
Lakeview Farms LLC is recalling Smilin' Bob's Key West Style Smoked Fish Dip in 8 oz and 15.5 oz containers due to potential Listeria monocytogenes contamination. The product was distributed to five distributors in Florida.
Conah Organic Enoki Mushrooms are recalled due to Listeria monocytogenes contamination detected by the California Department of Public Health. The affected product was distributed to California, Texas, and Arizona.
Magellan Diagnostics is recalling the LeadCare Ultra Blood Lead Test Kit due to control test failures causing potential underestimation of blood lead levels in patient samples. The recall involves 441 kits with worldwide distribution.
DiBAR LABS Hand Sanitizer (70% ethyl alcohol) in 16 FL OZ and 8 FL OZ bottles is being recalled nationwide because other lots and products made under the same conditions were found to contain methanol.
Interstate Food Products is recalling Little Hatch's Jalapeno Cream Cheese (14 oz.) due to Listeria monocytogenes contamination and undeclared soy lecithin. The product was distributed across multiple states.
Interstate Food Products is recalling Little Hatch's Queso (13.5 oz containers) because samples tested positive for Listeria monocytogenes and the product contains undeclared soy lecithin.
Xtreme Outdoors is recalling 2021 MyPod travel trailers because a support bracket may be insufficient, potentially causing the trailer shell to detach and create a road hazard.
Philips CT fluoroscopy monitor brackets may detach from suspension arms due to unrecognized shaft wear, risking the monitor falling and causing serious injury to patients, operators, or bystanders.
H & H Products Company is recalling Hartley's brand Worcestershire sauce in 1 gallon bottles and 50 gallon drums because the product labels do not declare the presence of fish (anchovies), a major allergen.
Cuisine Solutions is recalling JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper Sous Vide Plant Egg Bites because the product contains undeclared egg and milk allergens that are not listed on the label.
Tulkoff Food Products Inc. is recalling Tulkoff Spicy Kimchi Aioli (18 fl oz) due to undeclared soy and wheat allergens. The product was distributed in New Jersey, Pennsylvania, and Maryland.
Philips is recalling 1,301 Monitor Bracket Assemblies used in CT and PET/CT imaging systems worldwide due to potential shaft wear that could cause the monitor to detach from the ceiling mount and fall, posing injury risk.
Synaptive Medical is recalling 1,291 Trackable Suction Sets for visible metal burrs and filings along the inner suction tube. The defect may contaminate the surgical field or cause injury.
Spes Medica is recalling SNS Disposable Urethral Catheter Electrodes due to possible deviations in the ethylene oxide sterilization process. The recalled units may not be adequately sterilized, posing a potential infection risk to users.
Edwards Lifesciences is recalling 1,679 units of Edwards VAMP Jr. 6 in blood management systems (lot 63445142, 63630816) due to potential pressure tubing detachment.
One Twenty Clothing Company is recalling Sovereign Athletic-branded children's robes that fail to meet federal flammability standards for sleepwear, posing a burn hazard to children.
Wegmans is recalling Somerdale Red Dragon Cheddar Cheese because the label does not declare wheat from ale wash used in production. Consumers with wheat allergies or sensitivities are at risk.
Cuisine Solutions is recalling JUST Egg Inspired by Japan Portobello plant-based egg bites because they contain undeclared egg and milk. Consumers with allergies or sensitivities to these allergens should not consume the product.
Cuisine Solutions is recalling JUST Egg Inspired by India Curry, Broccoli, Cauliflower, Coconut Milk, Lemongrass Sous Vide Plant Egg Bites due to undeclared egg and milk allergens. The product was distributed nationwide.
Philips is recalling 1,301 Monitor Bracket Assemblies due to shaft wear that could cause the assembly to detach from the ceiling suspension arm. This could result in the monitor falling and causing serious injury to patients, operators, bystanders, or service personnel.
Wayfarer is recalling 2017-2021 recreational vehicles because valve stem extenders may rub against wheel liners, potentially causing sudden tire pressure loss and increasing crash risk.
Shenzhen Dianliangzhihui Tech Co. is recalling aftermarket Lasfit LED headlight bulbs sold on Amazon because they create excessive glare, increasing crash risk.
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter, Metris, and Freightliner Sprinter vehicles because seat belt retractors may deactivate early, preventing child restraints from securing properly.
Philips North America is recalling CT system monitor bracket assemblies due to shaft wear that could cause the bracket to detach from the suspension arm, potentially allowing the monitor to fall and cause serious injury.
Philips has recalled 1,301 Monitor Bracket Assemblies for CT systems worldwide due to shaft wear that could cause monitors to detach and fall, potentially injuring patients, operators, or service personnel.
Edwards Lifesciences is recalling the TruWave 3 cc/VAMP Jr pressure monitoring set (Lot #63598812) due to a potential risk that the pressure tubing may detach from the blood sampling system.
Quidel Corporation is recalling approximately 29,787 kits of the Lyra SARS-CoV-2 Assay due to a theoretical risk that samples with very high viral loads could produce false negative results. No false negatives have been formally reported.
Bard Access Systems is recalling PowerPICC catheter convenience kits with incorrect guidewires. Kits labeled as containing 70 cm guidewires actually contain 50 cm guidewires, which could affect proper catheter placement.
GE Healthcare is recalling Revolution EVO, Optima CT660, and Optima CT680 CT Systems due to improperly loaded software that may result in additional X-ray radiation exposure to patients.
Remote Diagnostic Technologies is recalling Tempus Pro patient monitors (Trizeps 7 variant) that can produce error states when unplugged while connected to a specified laryngoscope device. No injuries have been reported.
Medtronic is recalling 3 Endurant II/IIs Stent Graft Systems due to an incorrect stentstop assembly component in the delivery system. The defective devices use an 18-French assembly instead of the required 20-French component.
Philips is recalling 1,301 monitor bracket assemblies used with CT systems due to shaft wear that could cause monitors to fall, potentially injuring patients, operators, bystanders, or service personnel.
Spes Medica is recalling Tripolar Hooked Stimulation Probes due to possible deviations in the ethylene oxide sterilization process. The affected devices were distributed to healthcare facilities in California, Massachusetts, and South Carolina.
NeuMoDx Molecular Inc. is recalling certain cartridge lots that may produce false positive diagnostic results. Affected healthcare providers should verify tests performed with these cartridges and contact the manufacturer for guidance.
Exactech is recalling Humeral Augmented Tray (HAT) orthopedic implant components because the retaining ring may disengage during use. The recall affects 36 devices distributed in six U.S. states.
Edwards Lifesciences is recalling 990 units of the Edwards TruWave (30 cc)/VAMP Jr Kit pressure monitoring set because the pressure tubing may detach from the blood sampling system. Healthcare facilities should discontinue use.
Edwards Lifesciences blood management system (VJ0990) pressure tubing may detach from the blood sampling system during use. The recall affects 2,000 units distributed across the U.S., Canada, UK, and Italy.
Flowonix Medical is recalling physician order forms for Prometra infusion pumps due to ambiguous wording that could be misinterpreted as instructions to reuse previously extracted medication, posing an infection risk.
Edwards Lifesciences is recalling Edwards TruWave (3 cc)/VAMP Jr Pressure Monitoring Sets (Lot 63545959) due to a potential risk that pressure tubing may detach from the blood sampling system.
Edwards Lifesciences is recalling its pressure monitoring set due to potential tubing detachment. Approximately 460 units distributed across North America and Europe are affected.
Philips is recalling 1,301 monitor bracket assemblies for CT imaging systems due to shaft wear that could cause detachment and fall of the monitor. This could result in serious injury to patients, operators, and staff.
One lot of PORTEX ULTRperc Percutaneous Dilation Tracheostomy Kit (Lot 4072715) was incorrectly labeled as 7.0mm when it is 9.0mm. The 40 units were distributed in Pennsylvania, Michigan, Maryland, and Florida.
Cuisine Solutions is recalling JUST Egg Inspired by Mexico Roasted Poblanos Sous Vide Plant Egg Bites nationwide due to undeclared egg and milk allergens. Consumers with allergies to egg or milk who purchased these products should not consume them.
The Leavitt Corporation is recalling URBAN MEADOW brand dry roasted unsalted peanuts (16 oz jars) because the product may contain high levels of aflatoxin, a naturally occurring toxin that can cause serious health effects.
Philips medical imaging equipment monitor bracket assemblies may detach due to unrecognized shaft wear, risking the monitor falling and causing serious injury to patients, operators, or bystanders.
Philips monitor bracket assemblies for CT/PET imaging systems may detach due to shaft wear, posing a risk of the monitor falling and causing serious injury to patients, operators, or bystanders.
Edwards Lifesciences is recalling a pressure monitoring set due to potential detachment of the pressure tubing from the blood sampling system. The recall affects 290 units distributed across multiple US states and international locations.
Philips is recalling 1,301 monitor bracket assemblies for CT/PET-CT imaging systems due to shaft wear that could cause detachment from the suspension arm, potentially resulting in the monitor falling and serious injury.
Spes Medica has recalled SNS Disposable Urethral Catheter Electrodes due to possible deviations in ethylene oxide sterilization processes. The recall affects one lot distributed in California, Massachusetts, and South Carolina.
Philips CT fluoroscopy monitors may develop bracket shaft wear that could lead to the monitor detaching and falling while attached to cables.
SPINEART SA is recalling 44 units of PERLA TL Lateral Connector Open spinal fusion connectors distributed in the U.S. due to external labels that incorrectly list the rod size.
Spes Medica is recalling Dragonfly Laryngeal Surface Electrodes due to possible deviations in ethylene oxide sterilization parameters. The affected lots are LS20E2538I and 110320C, distributed to select US states.
Philips medical imaging monitors with worn bracket assembly shafts may detach from ceiling suspensions and fall on patients, operators, or staff. No injuries have been reported.
Bard Access Systems is recalling 180 units of 5Fr PowerPICC Catheter kits because they contain incorrect micro-introducers.
Carefusion is recalling a batch of MaxPlus Bi Fuse extension sets due to leakage defects. The affected units failed validation testing for leakage and were inadvertently released to the Tennessee market.
HoYu (US) Logistics Inc is recalling QiYu Hand Sanitizer (75% ethyl alcohol) because the product is subpotent. The recall affects 30,880 bottles distributed nationwide.
Spes Medica is recalling Dragonfly Laryngeal Surface Electrodes due to possible deviations in ethylene oxide sterilization process. Affected lot LS20G3274I was distributed in California, Massachusetts, and South Carolina.
Edwards Lifesciences is recalling Edwards TruWave pressure monitoring sets due to potential tubing detachment from the blood sampling system. No illnesses or injuries have been reported.
El Presidente Foods is recalling Just Nuts Japanese Style Peanuts (6.17 oz bags, Lot 317-20, expiring July 19, 2021) distributed in California because FDA inspection found the peanuts contained non-approved Red #6 dye.
Northwood is recalling specific 2019 Nash and Arctic Fox trailers because a stove component may cause a gas leak, increasing fire risk.
Guangzhou Yorkim Trading Co., Ltd is recalling Yorkim R7 H11 LED bulbs sold on Amazon because they create excessive glare, failing federal safety standards.
Tyson Foods is recalling approximately 8.9 million pounds of ready-to-eat chicken products due to possible Listeria monocytogenes contamination linked to illnesses and one death.
Daimler Trucks is recalling 2022 Freightliner Custom Chassis MT45 vehicles because an undersized rear leaf spring eye may break and detach, creating a road hazard.
Marion Body Works is recalling 2017-2020 Spartan Fire MetroStar and Gladiator vehicles because a fuel rail leak could cause a fire.
Newmar recalls 2017-2021 Mountain Aire, New Aire, Ventana, and Dutch Star RVs with Cummins diesel engines for a fuel rail sealing defect that can leak, increasing fire risk. Owners should contact Newmar for free inspection and repair.
Mercedes-Benz is recalling specific 2018-2021 models because LED headlights may have been incorrectly adjusted during repair, reducing visibility and increasing crash risk.
Braxton Creek is recalling 2020 and 2021 LX and BX travel trailers with Dometic cooking stoves due to an overtightened saddle valve bolt that can damage the o-ring seal and cause a continuous gas leak, posing a fire risk.
General Motors is recalling 2017-2019 Chevrolet Silverado and GMC Sierra trucks with Duramax diesel engines due to an electrical short-circuit risk in the engine-block heater that could cause a fire.
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