Archive
595 recalls were announced in August 2024.
Of the 595 recalls this month scored against our rubric, 3% are Critical, 23% are Severe.
Which agencies issued them
Medline recalls suction canister liners with dimensional variation that may cause fitting difficulties.
Medline Industries is recalling 1500ML soft liners due to dimensional variations that may make fitting into the outer canister more difficult. No injuries have been reported.
HAND-I-SAN No-Rinse Hand Sanitizer is being recalled due to manufacturing process deviations involving the use of non-sterile water in production. The product was distributed nationwide and to Canada.
Medline Industries is recalling 75,098 medical procedure kits due to slight dimensional variations that may cause difficulty fitting into their outer canisters. No injuries or illnesses have been reported.
Kentucky Trailer is recalling 2022-2024 MV and PV truck bodies because the upper cargo floor may not be secured properly, allowing crossmembers to loosen and detach.
Jayco is recalling certain 2023-2025 Entegra Ethos, Ethos LI, Arc, Jayco Swift, Swift LI and Comet motorhomes because radio software may prevent the rearview image from displaying, failing FMVSS 111.
USK Internacional is recalling certain tie rod and drag link assemblies due to improperly heat-treated ball studs that may break, potentially causing a loss of steering control.
Toyota is recalling certain 2023-2024 Sequoia Hybrid vehicles with a tow hitch cover attached to the rear bumper because the cover may come loose and detach from the vehicle.
ATC is recalling 2021-2023 Commercial Office trailers with CK7G generators because loose fuel lines may leak, increasing fire risk.
GE Appliances is recalling certain recreational vehicle air conditioners because the soft start device may fail and overheat, increasing the risk of a fire.
ATC is recalling 2021-2023 Commercial Office trailers equipped with CK7G generators because a failing exhaust port may cause a fire.
Jaguar is recalling 2,760 2019 I-PACE vehicles because the high-voltage battery may overheat, increasing the risk of a fire. Owners should park outside and limit charging to 80% until repairs are complete.
Great Dane is recalling 2025 Everest SS refrigerated trailers because improperly welded support gear bracing mounts may cause the trailer to collapse.
Navico Group is recalling Progressive RSM-30 and PSK-30 surge protectors for recreational vehicles because the ground contact may fail, increasing the risk of electrical shock.
Ford is recalling certain 2021-2022 vehicles with 2.7L or 3.0L Nano EcoBoost engines because the engine intake valves may break, resulting in engine failure and loss of drive power.
Ford is recalling 2024 Transit vehicles because incorrect front axle weight labels may lead to overloading, increasing the risk of steering failure and crashes.
Ford is recalling certain Lincoln Corsair, Escape, Mustang and Explorer vehicles because fuel injectors may have been assembled without O-ring support discs. 24 units affected.
Forest River is recalling certain 2024 Salem and Wildwood travel trailers because the tire may contact the outrigger, causing the tire to fail. 34 units are affected.
Forest River is recalling certain 2024-2025 Salem SBF325RL and Wildwood WBF325RL travel trailers because the tires may contact chassis components, causing tire failure.
Head Rush Technologies is recalling about 220 TRUBLUE Speed Auto Belay Devices because the backup brake can fail to activate, posing a fall hazard and risk of serious injury or death. Consumers should immediately stop using the devices and contact the manufacturer for a free inspection and repair.
McNeilus is recalling 2015-2024 Zero Radius refuse trucks because the side loader arm may not be properly secured, increasing crash risk.
Siemens is recalling about 3,910 SolarReady Meter Combos because an interior connection can overheat and pose a fire hazard. The firm has received eight reports of overheating, including one localized fire, but no injuries.
Endera Motors is recalling 2022-2023 school buses because emergency exit label text is too small to read, potentially delaying evacuation.
Endera Motors is recalling 2022-2023 school buses because the rear emergency exit door may close unexpectedly, increasing injury risk.
Shawshank LEDz is recalling approximately 9,600 Squeeze Plush Ball toys sold at Ace Hardware because the toys contain liquid and glitter that can splash out if the membrane ruptures, potentially injuring a child's eyes and face.
Freshire Farms jalapenos packaged in 8-ounce bags are being recalled due to potential contamination with Listeria monocytogenes. The recall affects 2,298 cases distributed across nine states.
RS Hanline and Company Inc is recalling Freshire Farms green peppers due to potential Listeria monocytogenes contamination. The recall affects 850 cases distributed across nine states.
Metro Produce Distributors is recalling 66 units of Lunds & Byerlys Pico de Gallo/Guacamole Dip distributed in Minnesota due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
ICU Medical is recalling Plum 360 Infusion System replacement batteries due to a manufacturing defect that may cause loss of capacity and decreased runtime earlier than expected. Approximately 11,961 units were distributed worldwide.
ICU Medical is recalling 130,826 units of Plum 360/A+ spare batteries due to a manufacturing defect that causes earlier-than-expected battery capacity loss and reduced runtime.
ICU Medical is recalling Plum A+ and Plum A+3 infusion pump batteries due to a manufacturing defect that may cause premature capacity loss and reduced runtime. Approximately 14,744 units were distributed worldwide.
Lunds & Byerlys Deli Guacamole (Item 85999, 56 oz) may be contaminated with Listeria monocytogenes. Twenty-eight units with a Use By date of 02-AUG-24 were distributed in Minnesota.
North Fish USA is recalling Cold Smoked Capelin packages due to potential Clostridium botulinum contamination in uneviscerated fish. The affected products were distributed in Georgia and New York.
Foppen Smoked Norwegian Salmon Slices (8.1oz vacuum foil packages) are recalled due to potential contamination with Listeria monocytogenes. The recall affects 747 cases distributed across 15 U.S. states.
Defibtech is recalling the RMU-2000 Automated Chest Compression Device because a motor defect may cause the device to stop delivering compressions, potentially delaying critical therapy and resulting in patient injury or death.
RS Hanline and Company Inc is recalling Poblano peppers in multiple package formats due to potential Listeria monocytogenes contamination. The affected product was distributed across nine U.S. states.
RS Hanline and Company Inc is recalling Freshire Farms Green Beans due to potential Listeria monocytogenes contamination. Approximately 1150 cases were distributed across nine states.
Van Leeuwen Ice Cream is recalling Pumpkin Cinnamon Roll non-dairy frozen dessert (14 oz) due to undeclared peanuts. The allergen poses serious risk to consumers with peanut allergies.
Metro Produce Distributors is recalling Lunds & Byerlys Fresh Guacamole Dip due to potential Listeria monocytogenes contamination. The affected product has a Use By date of 02-AUG-24 and was distributed in Minnesota.
Metro Produce Distributors is recalling 121 units of Lunds & Byerlys Spicy Guacamole Dip because it may be contaminated with Listeria monocytogenes. The affected product was distributed in Minnesota.
Publix Super Markets is recalling 2,786 units of Boars Head Grab and Go Wedge Ham products due to potential Listeria monocytogenes contamination. The affected products were sold at retail locations in Florida and Georgia.
Metro Produce Distributors is recalling Lunds & Byerlys Smokin' Guacamole Dip due to possible Listeria monocytogenes contamination. The 10 oz product was distributed in Minnesota.
RS Hanline and Company Inc is recalling green peppers due to potential Listeria monocytogenes contamination. The recall affects peppers distributed across nine states.
OEM Systems is recalling certain 2024 Chevrolet Silverado vehicles because the rear bumper mounting bracket may not be sufficient for towing, allowing a trailer to detach.
Merit Medical convenience kits containing defective plastic syringes are being recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects approximately 4,027 kits distributed nationwide.
Becton Dickinson & Co. is recalling the BD Kiestra Urine Culture Application due to a software issue that may cause inaccurate bacterial colony counts. This could impact patient diagnosis and treatment decisions.
Beckman Coulter has recalled 183 DxI 9000 Access analyzers due to a software issue that causes delays in test result reporting. When connected to a Laboratory Automation System, software versions 1.17 and below send out-of-sequence messages, potentially delaying patient treatment.
Merit Medical convenience kits containing recalled plastic syringes have quality issues including leaks and breakage that may pose risks during vascular and cardiac procedures. Approximately 5,700 affected kits were distributed nationwide.
Merit Medical is recalling convenience kits containing syringes with quality issues including leaks and breakage that may pose a risk to patients receiving intravenous fluid administration.
Aurora Series surgical light heads are recalled due to cracked welds on the frame. The defects can cause the frame to sag, housing to crack, or the light head to detach.
Merit Medical convenience kits containing recalled syringes are subject to a nationwide recall due to quality defects including leaks and breakage that may pose risks to patient health.
Merit Medical is recalling paracentesis procedure kits nationwide containing syringes with identified leaks and breakage. The defects may pose a risk to patient health during medical procedures.
Merit Medical convenience kits containing recalled syringes have quality issues including leaks and breakage that may pose a risk to patient health. The recall affects 2,388 kits distributed nationwide.
Full Circle Coconut Milk Chocolate Almond Crunch frozen dessert is recalled due to undeclared cashews. Product labels show mismatch: carton states 'coconut milk' but top states 'cashew milk,' and product contains cashew milk.
SUBCO FOODS INC is recalling 137 cases of Fox's u-bet Sugar-Free Chocolate Flavored Syrup due to elevated pH and water activity levels indicating potential microbiological contamination and food-borne illness risk.
Merit Medical is recalling 7,442 convenience kits containing defective syringes that may leak or break, posing a risk to patient health.
Merit Medical is recalling 69 convenience kits containing defective syringes that may leak or break, potentially risking patient safety during medical procedures. The kits were distributed nationwide.
Palodex Group Oy recalls the Orthopantomograph OP300 dental x-ray system due to a testing software defect that may allow devices with poor image repeatability to be distributed.
DKK Dai-Ichi Shomei Co., Ltd. is recalling 822 Aurora surgical light heads due to a weld defect that could cause the light head to sag, crack, or detach during use.
RS Hanline and Company Inc is recalling jalapeno peppers due to potential contamination with Listeria monocytogenes. The affected products were distributed across nine states.
FDC Limited recalls Timolol Maleate eye drops (362,544 bottles) nationwide due to a manufacturing defect: a yellow spike from the cap lodged in the nozzle, posing a risk of eye injury.
Merit Medical convenience kits containing plastic syringes are recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health. The affected kits are used for vascular and cardiac procedures.
DKK Dai-Ichi Shomei is recalling 293 Aurora surgical light heads because the frame welds can crack, potentially causing the light head to detach during use. No injuries have been reported.
Merit Medical convenience kits containing plastic syringes are recalled due to leaks, breakage, and quality issues that may pose risks to patients undergoing cardiac and vascular procedures.
Boston Scientific spinal cord stimulation implants may reset during routine charging, causing brief loss of therapy. Patients may experience undesired sensations when stimulation restarts, potentially leading to surgical intervention requests.
Merit Medical is recalling 1,390 convenience kits containing plastic syringes with identified quality issues including leaks and breakage. The kits, distributed nationwide, may pose a risk to patient health.
DKK Dai-Ichi Shomei is recalling 555 Aurora 7 surgical light heads because frame welds can crack, causing the frame to sag, the housing to crack, or the light head to detach.
Pariva LLC is recalling Pariva Marinated Labneh Bites Mild Tandoori due to potential mold contamination. Affected products were distributed in Massachusetts, Maine, New Hampshire, Rhode Island, New York, New Jersey, and Connecticut.
Merit Medical is recalling convenience kits containing syringes with quality defects including leaks and breakage that may pose patient safety risks in cardiac and vascular procedures.
Convenience kits from Merit Medical Systems containing recalled plastic syringes have identified quality issues including leaks and breakage that may pose a risk to patient health.
Pariva LLC is recalling Pariva Marinated Labneh Bites Za'atar (8 oz) due to potential mold contamination. The product was distributed in seven Northeast states with best-by dates in October or December 2024.
Merit Medical is recalling 3,631 catheter extractor convenience kits due to defective syringes with leaks and breakage. The identified quality issues may compromise patient safety during catheter removal.
Merit Medical is recalling medical convenience kits with defective syringes due to identified leaks, breakage, and quality issues that may pose a risk to patient health during procedures.
Cepheid specimen collection devices may leak after patient samples are inserted, creating risk of biohazard exposure and false positive test results. Affected devices are distributed in medical testing facilities worldwide.
Thoratec LLC is recalling 694 HeartMate 3 System Controllers because the UI membrane may lift along the housing, allowing fluid entry that could damage internal circuits and cause loss of power or pump failure.
Merit Medical convenience kits used in cardiac procedures contain plastic syringes with potential leaks and breakage. The defects were identified following an FDA Safety Alert issued March 19, 2024.
Merit Medical convenience kits containing plastic syringes are recalled due to leaks, breakage, and quality defects that may pose a risk to patient health. Approximately 3,647 kits were distributed nationwide.
Merit Medical convenience kits containing defective syringes are being recalled for leaks and breakage that may pose a risk to patient health.
Merit Medical is recalling 900 convenience kits containing plastic syringes due to identified leaks, breakage, and quality issues that may pose a risk to patient health.
Merit Medical is recalling convenience kits containing syringes with quality defects including leaks and breakage. The recalled kits may pose a risk to patients undergoing vascular and cardiac procedures.
EYE COMFORT CARE LLC is recalling the UNclog Eye Mask due to safety clips that may allow wires to detach, potentially causing electrical shorts and burn injuries.
A software anomaly causes the BioButton remote monitoring wearable device to report skin temperature readings slightly out of specification, affecting accurate health data collection in home and healthcare settings.
Alfa Supply is recalling Abby's Best Biscuit Mix due to undeclared wheat allergen on the product label. The product was distributed to California, Florida, Virginia, Washington, and Bahrain.
Bovine collagen peptide powder manufactured by Nanjing NutraBuilding Bio Tech is being recalled due to potential Salmonella contamination. Affected batches were distributed in Wisconsin.
Escape Trailer is recalling certain 2024 travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat. 248 units are affected.
Merit Medical convenience kits containing defective syringes have been recalled nationwide. Identified quality issues including leaks and breakage may pose risks during cardiac and vascular procedures.
Alamo Group is recalling specific Morbark trailers because loose wires in the power module may cause electrical arcing and fire.
Merit Medical's Prelude SNAP-H cardiac catheter kits are being recalled because their syringes may leak or break during use, potentially affecting cardiac procedures. No illnesses have been reported.
Merit Medical convenience kits containing plastic syringes have been recalled nationwide. The syringes have quality issues including leaks and breakage that may pose a risk to patient health.
SUBCO Foods is recalling Fox's u-bet Vanilla Flavored Syrup due to bloated bottles and elevated pH and water activity levels that indicate potential microbiological contamination and food-borne illness risk.
Ortho-Clinical Diagnostics is recalling VITROS Folate Reagent Pack due to fibrinogen precipitation causing delayed test results. The recall affects 18,467 units distributed worldwide.
Beckman Coulter is recalling 59 units of its Access 2 Immunoassay System Analyzer due to misaligned index wheels causing carousel motion errors that disable the analyzer and cancel patient tests.
Taro Pharmaceuticals recalled Hydrocortisone 1% & Acetic Acid 2% Otic Solution (lot AD12890) due to failed impurity specifications and lower-than-established active ingredient levels during stability testing.
Pariva LLC recalls Marinated Labneh Bites due to potential mold contamination. Approximately 4,261 units were distributed across seven states.
Argon Medical Devices recalls PICC catheters that are mislabeled. Packages marked 26G/1.9Fr x 30cm actually contain 26G/1.9Fr x 50cm catheters, which could delay procedures.
DRG International is recalling Salivary Testosterone ELISA kits (Model SLV-3013) due to out-of-range quality controls that invalidate test runs and delay patient results. The recall affects 257 units distributed nationwide in six states.
Continental is recalling specific ProContact GX AO tires because a design flaw may cause excessive heat buildup and belt separation, increasing crash risk.
Fisker is recalling certain 2023-2024 Ocean vehicles because the brake module software may cause an unexpected reduction in regenerative braking, decreasing braking performance.
Motor Coach Industries is recalling 2021 D45CRTeLE vehicles because a software error may cause battery damage and increase the risk of fire.
Continental is recalling specific HDL2 DL+ tires because an incorrect rubber compound may cause the steel belt to separate, potentially leading to a loss of vehicle control.
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