Recalls in August 2026
600 recalls.
- Wheat Germ recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Whole wheat flour recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Tube Shaped Wheat Snack recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - 4X6 Wheat Snack recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - 10X10 Wheat Snack recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Milk Chocolate Covered Raisins recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Milk, Soy) - Tropical Trail Mix recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Peanuts, Almonds, Sulfites, Yellow#6) - Whole Wheat recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Textured Soy Protein recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Soy) - Wheat Bran recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Raw Shelled Pistachios recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Pistachios) - Shelled White Pine Nuts recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Pine Nuts) - Dried Pineapple Rings recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites) - Dried Diced Pineapple recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites) - Dried Pears recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites) - Dried Papaya Spears recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Yellow#6, Sulfites) - Dried Diced Papaya recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Yellow#6, Sulfites) - Bread Crumbs recall (El Ruisenor De Mexico, Inc.)
FoodClass IReported October 28, 2026 · undeclared allergen ingredient (Milk, Wheat, Sesame, Soy) - Pecans in Shell recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Pecans) - Walnut halves recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Walnuts) - Walnuts in Shell recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Walnuts) - Homestyle Poblano Mole recall (El Ruisenor De Mexico, Inc.)
FoodClass IReported October 28, 2026 · undeclared allergen ingredient (Sesame, Peanuts, Wheat, Soy, Sulfites) - Special Red Almond Mole Powder recall (El Ruisenor De Mexico, Inc.)
FoodClass IReported October 28, 2026 · undeclared allergen ingredient (Sesame, Peanuts, Wheat, Soy, Almonds, Walnuts, Yellow#5, Yellow#6, Red#40, Blue#2) - Roasted & Salted Mixed Nuts recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Cashew, Almond, Brazil Nut, Hazelnut, Pecan) - Air-Dried Apple Rings recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites) - Dried Mango Slices recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites, Yellow#6) - Dried Kiwi Slices recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites, Yellow#5, Blue#1) - Horchata Drink Mix recall (El Ruisenor De Mexico, Inc.)
FoodClass IReported October 28, 2026 · undeclared allergen ingredient (Milk) - Honey Nut Granola recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Almond, Cashew) - Harina de Trigo recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Almond Flour recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Almond) - All-Purpose Flour recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Jovy Gummy Worms recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1) - Jovy Gummy Worms Neon recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1) - Jovy Gummy Bears Regular recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1) - Jovy Gummy Bears Neon recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1) - Jovy Watermelon Gummy Rings recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Red#40) - Apple Rings recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared sulfites - Jovy Gummy Peach Rings recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6) - Dried Fruit Mix recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites, Yellow#6) - Fritura Rueda Papa / Potato Wheel Snack recall (El Ruisenor De Mexico, Inc.)
FoodClass IReported October 28, 2026 · undeclared allergen ingredient (Wheat) - Fritura Rueda / Wheat Wheel Snack recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Wheat, Yellow#5, Yellow #6,) - Fritura Lagrimita / Teardrop Wheat Snack recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Wheat, Yellow #6, Soy) - Fritura mixed dry fruit recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Wheat, Yellow #5, Yellow #6) - Soybeans recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Soy) - Dried Peaches recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites) - Churro Mix recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Egg, Wheat) - Whole Pitted Dried Apricots recall (El Ruisenor De Mexico, Inc.)
FoodClass IIReported October 28, 2026 · undeclared allergen ingredient (Sulfites) - Ground Shrimp recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (shrimp) - Dried Whole Shrimp recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (shrimp) - Raw In-Shell Peanuts recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Peanuts) - Butter Toffee Peanuts recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Peanuts, Milk) - Dried Cod recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Fish) - Hazelnuts in Shell recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Hazelnut) - Sliced Almonds recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Almond) - Roasted Whole Almonds recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Almond) - Chocolate Covered Almonds recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Almond) - Almonds in Shell recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Almond) - Hulled Sesame Seeds recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Sesame) - Black Sesame Seeds recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · undeclared allergen ingredient (Sesame) - Natural Sesame Seeds recall (El Ruisenor De Mexico, Inc.)
FoodClass IIIReported October 28, 2026 · various undeclared allergen ingredients (Sesame) - Ion Torrent Genexus Dx with software recall (Life Technologies Holdings Pte Ltd)
Medical deviceClass IIReported October 28, 2026 · DNA or RNA sequencing system software has vulnerabilities. - Techno-Path Multichem AE Unassayed Level 3 recall (TECHNO-PATH MANUFACTURING LTD.)
Medical deviceClass IIReported October 28, 2026 · A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.... - Techno-Path Multichem AE Unassayed Level 2 REF: AE622X recall (TECHNO-PATH MANUFACTURING LTD.)
Medical deviceClass IIReported October 28, 2026 · A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.... - Techno-Path Multichem AE Unassayed Level 1 REF:AE621X recall (TECHNO-PATH MANUFACTURING LTD.)
Medical deviceClass IIReported October 28, 2026 · A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.... - Medtronic Biopsy Needle Kit recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801075 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801074 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Medtronic NDI Passive Spheres REF: 8801071 recall (Medtronic Navigation, Inc.)
Medical deviceClass IIReported October 28, 2026 · Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect... - Think Surgical Square Driver REF: 109126 recall (Think Surgical, Inc.)
Medical deviceClass IIReported October 28, 2026 · Robotic system square drive failed to meet design specifications potentially resulting in pin becoming stuck in square driver or the pin wobbling during... - The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists recall (Radiometer Medical ApS)
Medical deviceClass IIReported October 21, 2026 · In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood... - Scout MD recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 21, 2026 · The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use. - Convenience Kits containing CONMED AirSeal Access Ports KIT ROBOTICS UROLOGY... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - IQ200 SPRINT recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - DxU 840m Iris recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control recall (Microgenics Corporation)
Medical deviceClass IIReported October 21, 2026 · Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone... - Generic Name: BioFire¿ Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel ... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - iFuse TORQ Implant System Model/Catalog Number: 10055T recall (SI-BONE, Inc.)
Medical deviceClass IIReported October 21, 2026 · The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. - NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number... recall (Neuronetics, Inc.)
Medical deviceClass IIReported October 21, 2026 · Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly. - Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number:... recall (Cadwell Industries Inc)
Medical deviceClass IIReported October 21, 2026 · Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the... - BD Phoenix Panel NMIC-306. Catalog Number: 449292. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - BD Phoenix Panel NMIC-312. Catalog Number: 449082. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to... - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related... - Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5... recall (The Better Bakehouse Snack Company)
FoodClass IReported October 14, 2026 · Undeclared Milk. - Intellijoint Navigation System: Workstation G2 Configured recall (Intellijoint Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro... - TufTex¿ Over-the-Wire Embolectomy Catheter recall (LeMaitre Vascular, Inc.)
Medical deviceClass IIReported October 14, 2026 · Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing. - T1 Patient Monitor. Operator's Manual: T1 Patient Monitor recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneView Series. Operator's Manuals: T5 / T8 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama... recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions