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
Classic Delight LLC is recalling 2,311 cases of Wakefield Bacon, Egg & Cheese Bagels (Item 514711) due to possible Listeria monocytogenes contamination. The affected product was distributed across 14 states.
GE Healthcare recalls CARESCAPE B650 patient monitors that may fail to power on after mains power loss following CPU timekeeper battery replacement, potentially delaying recognition of patient condition changes.
Medtronic recalls 26 units of CROME HF QUAD CRT-D implantable defibrillators worldwide due to weld cracks discovered during manufacturing quality control. Devices were contained before reaching patients.
Maquet Cardiovascular recalls VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems due to fluid ingress into the harvesting tool handle, which may prevent necessary cautery or cause unintended cautery during surgical procedures.
Siemens is recalling 4 AXIOM Vertix Solitaire medical imaging devices due to a short circuit in the touch display power supply that may cause overheating and fire. Units with serial numbers 1004, 1006, 1011, and 1014 are affected.
Medtronic is recalling 3 MIRRO MRI DR SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality checks. The defect was detected during manufacturing before devices reached patients.
SWOMOG children's two-piece pajama sets sold on Amazon.com from May 2022 through January 2024 violate federal flammability standards for children's sleepwear, posing a burn hazard. Consumers should stop use immediately and contact SWOMOG for a full refund.
ASPEN SURGICAL is recalling 1,900 units of the Endoscopic Kittner Blunt Dissecting Instrument (Model KT-9101) due to a potential defect in the sterile barrier seal.
Tiffin is recalling certain motorhomes because the wheel bolts for the spare tire may be missing. A spare tire without correct bolts could detach and increase crash risk.
Stryker is recalling 39 Hoffman LRF Wire Tensioner devices because the adjustment ring may loosen, preventing proper tension setting. No injuries reported.
Reyco Granning is recalling specific independent front suspension assemblies because lower control arm retention bolts may become brittle and break, posing an injury risk.
Merit Medical Systems is recalling Prelude Roadster Guide Sheaths due to an instructional defect. Older instructions directing tight connection assembly may cause over-tightening, leading to swivel nut detachment.
Daimler Trucks North America is recalling 2023-2025 Freightliner Custom Chassis S2C and S2RV trucks because brake lights may not illuminate during active brake assist events.
Penguin Natural Foods is recalling 'THE PERFECT CHOCOLATE CHUNK COOKIE MIX Cravings by Chrissy Teigen' because the product contains undeclared coconut. Consumers with coconut allergies face a serious health risk.
Lidl US TRADING is recalling approximately 2,000 units of Chef Select 2 Herb Baguettes due to undeclared wheat and milk allergens resulting from foreign language labeling. Consumers with wheat or milk allergies should not consume this product.
Siemens is recalling 3 Multix TOP I PRO radiographic X-ray tables due to a short circuit in the Touch Display power supply unit that may cause overheating and fire.
Fresh Catch Inc. is recalling Yellowfin Tuna for high histamine levels. No illnesses have been reported.
Medtronic recalled 14 COBALT HF QUAD CRT-D MRI SureScan implantable defibrillators due to a weld crack manufacturing defect detected during quality control testing.
Medtronic recalls 9 units of CROME VR MRI SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality control leak testing.
Medtronic is recalling 26 MIRRO MRI DR SureScan Implantable Cardioverter Defibrillators due to a manufacturing defect involving a weld crack that could affect device function.
Maquet Cardiovascular recalls VasoView HemoPro 2 vessel harvesting systems due to potential fluid ingress that may prevent or unintentionally activate cautery function. The recall affects 430,037 units distributed worldwide.
Classic Delight LLC is recalling 1,366 cases of Wakefield Ham, Egg & Cheese Muffins due to possible Listeria monocytogenes contamination. The affected products were distributed across 14 states.
Pfizer is recalling specific lots of Buprenorphine Hydrochloride Injection due to potential incomplete crimp seals that could compromise product sterility. Patients using affected lots should consult their healthcare provider.
Classic Delight LLC is recalling Wakefield Sausage, Egg & Cheese Biscuits (Item 514712) due to possible Listeria monocytogenes contamination. The affected products were distributed in 14 states.
Classic Delight LLC is recalling 1,250 cases of Wakefield Chicken & Cheese Kaiser Rolls due to possible Listeria monocytogenes contamination. The affected products were distributed across 14 states.
Medtronic is recalling 4 COBALT VR MRI SureScan implantable cardioverter defibrillators due to a manufacturing defect involving a weld crack identified during quality control testing.
Classic Delight LLC is recalling Wakefield Southern Chicken Biscuit (Item 176594) due to possible Listeria monocytogenes contamination. The product was distributed in 14 states with multiple affected lot numbers.
GE Healthcare is recalling certain CARESCAPE Canvas patient monitors that may fail to display vital signs after a power loss if the CPU battery has been replaced. This could delay recognition of changes in patient condition.
Classic Delight Breaded Chicken Waffle (Item 7626) for institutional use is being recalled due to possible contamination with Listeria monocytogenes. The recall affects 644 cases distributed to institutions in 14 states.
One lot of Sight OLO CBC Test Kit is being recalled due to bacterial contamination that causes artificially elevated platelet counts. The affected kits may produce inaccurate test results.
FDA is recalling 45 NovaGuide 2 Intelligent Ultrasound systems due to a defective grounding cable that could become disconnected and cause electrical shock, electrical interference, or equipment malfunction.
The CDC Influenza A/H5 Subtyping Kit's H5b component may fail to amplify, resulting in inconclusive results. 191 units were distributed nationwide.
Contract Pharmacal Corporation is recalling 14,616 bottles of Extra Strength Acetaminophen 500mg tablets due to discoloration appearing as brownish tablets. The affected lot was distributed in Michigan.
The tip holder portion of Titan Blis-Sonic Scaler tips may be oversized, preventing proper seating in the scaler handpiece. This defect could result in the tip becoming loose during use.
Cook Incorporated is recalling 15 units of a multipurpose drainage catheter due to product labels stating incorrect expiration dates that extend beyond the devices' true expiration, creating a risk of expired device use.
NeilMed Pharmaceuticals is recalling 20,370 bottles of SinuFrin Quick Relief Decongestant (Lot SD134) nationwide due to sub-potency. No illnesses have been reported.
Mack Trucks is recalling 2025 LR, Granite, and Pinnacle vehicles because a tie rod assembly ball stud may fail, creating a road hazard and increasing crash risk.
A battery management system failure in 2023-2024 Fisker Ocean vehicles can cause sudden loss of drive power. Fisker will replace the affected pumps at no cost.
Vermeer is recalling 84 units of the 2024 BC1200XL brush chipper because axle mounting bolts may not be properly tightened, posing a crash risk.
ARBOC is recalling 2023-2024 Spirit of Freedom vehicles because the seat recliner mechanism may not engage, increasing injury risk in a crash.
Forest River is recalling 2023-2024 Starcraft Starlite buses because emergency exit handles are not easily accessible, potentially delaying passenger evacuation during emergencies.
Spartan Fire is recalling 2023-2025 Gladiator, Metro Star, and KME Panther vehicles because lower control arm bolts may break and become projectiles.
Honda is recalling 2024 CR-V vehicles because the tires are missing required date code markings on the tire identification number. This prevents owners from identifying recalled tires and increases crash risk.
E-One is recalling 2024 Cyclone N and Typhoon N vehicles because lower front suspension control arm bolts may become brittle and break, posing an injury risk.
Volvo Trucks is recalling 2025 VHD and VN trucks because a tie rod ball stud may fail, creating a road hazard and increasing crash risk.
Certain 2024 Nissan Sentra vehicles have windshield air bubbles on the front lower driver's side that can obscure the Vehicle Identification Number. This defect prevents owners from clearly identifying their vehicle and may prevent recall recognition.
Lucid is recalling certain 2022 and 2023 Air vehicles due to a software fault that could disconnect the high voltage system while driving, causing loss of drive power and increasing crash risk. A free over-the-air software update is available.
Looking for a different month? Back to 2024.