Recalls in August 2026 (page 5)
600 recalls.
- Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump... recall (BD SWITZERLAND SARL)
Medical deviceClass IReported September 23, 2026 · Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance. - DuoGlide Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - Power-Trialysis Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - Alfalfa recall (International Sprout Holdings, Inc)
FoodClass IReported September 16, 2026 · Potential E. coli and Salmonella contamination - Prolon Everyday Apulian Almond & Cocoa Spread recall (L-Nutra Inc)
FoodClass IIReported September 16, 2026 · Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio. - Fannie May & XO Marshmallow Pixie S'mores Collection recall (Ferrero USA)
FoodClass IIReported September 16, 2026 · Undeclared milk and pecans - Crown Farms Dried Suri Cut recall (EURO FOODS GROUP USA NJ INC)
FoodClass IReported September 16, 2026 · The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying. - Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower recall (EXOTIQUE FOODS CANADA)
FoodClass IReported September 16, 2026 · Undeclared Wheat. - 0.9% Sodium Chloride Injection recall (B BRAUN MEDICAL INC)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene - Epinephrine Injection recall (American Regent, Inc.)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and... - Dextrose Injection recall (Baxter Healthcare Corporation)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution. - Fluphenazine Hydrochloride Tablets recall (Ajanta Pharma USA Inc)
DrugClass IIIReported September 16, 2026 · Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result... - Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution recall (ImprimisRx NJ LLC)
DrugClass IIIReported September 16, 2026 · Subpotent Drug - Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Bicarbonate Powder REF: DB+201-2.1 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser... recall (Lutronic Corporation)
Medical deviceClass IIReported September 16, 2026 · Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in... - Bravo CF capsule delivery device recall (Given Imaging Ltd.)
Medical deviceClass IReported September 16, 2026 · Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus... - Frankie's Organic Plant-Based Puffs Vegan Cheddar recall (Marina Del Rey Foods inc.)
FoodClass IReported September 9, 2026 · Product tested positive for undeclared milk. - Organic Cheddar Type Seasoning recall (Savor Seasonings LLC)
FoodClass IReported September 9, 2026 · Product tested positive for undeclared milk allergen. - THE HAMPTON GROCER brand recall (THE HAMPTON GROCER)
FoodClass IReported September 9, 2026 · Product may be contaminated with Salmonella. - Weis recall (WEIS MARKETS, INC.)
FoodClass IIReported September 9, 2026 · Product has high patulin levels - Prince PAN DE MANTECA recall (Prince Bakery Inc)
FoodClass IIReported September 9, 2026 · Milk is not declared in the Contains statement. - Prince Sesame FRENCH BREAD recall (Prince Bakery Inc)
FoodClass IIIReported September 9, 2026 · Sesame is not declared in the ingredient statement but is declared in the statement of identity. - Prince ITALIAN BREAD recall (Prince Bakery Inc)
FoodClass IIIReported September 9, 2026 · Sesame is not declared in the ingredient statement but is declared in the statement of identity. - Prince ITALIAN BREAD recall (Prince Bakery Inc)
FoodClass IIIReported September 9, 2026 · Sesame is not declared in the ingredient statement but is declared in the statement of identity. - Item #DIPSAU0205RFS Salsa Autentica 5 lb. packaged in round plastic container. recall (Ron's Home Style Foods, Inc.)
FoodClass IReported September 9, 2026 · Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella - Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic container. recall (Ron's Home Style Foods, Inc.)
FoodClass IReported September 9, 2026 · Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella - Glutathione 200 mg/mL recall (OPTIMAL BALANCE PHARMACY)
DrugClass IReported September 9, 2026 · Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. - 0.9% Sodium Chloride Injection USP 500 mL recall (Baxter Healthcare Corporation)
DrugClass IReported September 9, 2026 · Presence of particulate matter: Particulates identified as fiberglass - Prasugrel HCI recall (Golden State Medical Supply Inc.)
DrugClass IIReported September 9, 2026 · Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution - Buprenorphine Sublingual Tablets recall (American Health Packaging)
DrugClass IIIReported September 9, 2026 · Labeling: Label Mix-up - Prasugrel Tablets recall (Mylan Pharmaceuticals Inc)
DrugClass IIReported September 9, 2026 · Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria - Revcovi recall (Chiesi USA, Inc.)
DrugClass IIIReported September 9, 2026 · Failed Stability Specifications: Out of specification stability result for the protein concentration profile. - 2% Chlorhexidine Gluconate* Cloth recall (Sage Products, LLC)
DrugClass IIReported September 9, 2026 · Cross Contamination with Other Products - traZODone Hydrochloride Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported September 9, 2026 · Presence of Foreign Tablets/Capsules - Trokendi XR recall (Supernus Pharmaceuticals, Inc.)
DrugClass IIIReported September 9, 2026 · Failed dissolution specifications. - Carton label: Mycophenolate Mofetil for injection recall (Mylan Pharmaceuticals Inc)
DrugClass IIReported September 9, 2026 · Failed Dissolution Specifications - Broadway Joe's Pain Cream recall (Lexia LLC)
DrugClass IIReported September 9, 2026 · CGMP Deviations: Potential contamination of raw material - Broadway Joe's Pain Cream recall (Lexia LLC)
DrugClass IIReported September 9, 2026 · CGMP Deviations: Potential contamination of raw material - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg recall (Bionpharma Inc.)
DrugClass IIIReported September 9, 2026 · Presence of Foreign Tablets/Capsules - Daptomycin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vancomycin Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vasopressin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Phosphate in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Nexterone recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - CARDENE IV recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Pantoprazole Sodium in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vasopressin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Famotidine Injection in Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Daptomycin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - MYXREDLIN recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vancomycin Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog... recall (B Braun Medical Inc)
Medical deviceClass IIReported September 9, 2026 · Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. - 5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips Brilliance. Models: Brilliance iCT recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Clear glass bottle with black screw lid with multi label which reads in part as... recall (Africando Foods LLC)
FoodClass IIReported September 2, 2026 · Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list - Horizon Organic ORG ASEP CHOC MILK 1% 8OZ 12 CT recall (Horizon Organic Dairy, LLC)
FoodClass IIReported September 2, 2026 · Product has the potential to be spoiled. - Mehadrin Chocolate Leben recall (UPSTATE NIAGARA COOPERATIVE)
FoodClass IIReported September 2, 2026 · Product may have been improperly pasteurized. - Jalapeno Ranch recall (Jaime's Foods ATX, LLC)
FoodClass IReported September 2, 2026 · Undeclared Egg Allergen - Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Marketside Tomato Bisque Soup Kit recall (CUISINE, KETTLE)
FoodClass IIReported September 2, 2026 · Product had a presumptive positive test result for Listeria monocytogenes - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Black Cherry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Tangerine recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Grape recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bar Watermelon recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB recall (Sirna and Sons Produce, Inc)
FoodClass IReported September 2, 2026 · Potential Salmonella Javiana contamination - Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package... recall (H & U Inc. dba Sun Noodle)
FoodClass IReported September 2, 2026 · Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish... - Lactated Ringer's Injection USP recall (B BRAUN MEDICAL INC)
DrugClass IReported September 2, 2026 · Presence of Particulate matter. - Ramipril Capsules USP recall (Hikma Pharmaceuticals USA INC.)
DrugClass IIReported September 2, 2026 · Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU). - Tyenne recall (Fresenius Kabi USA, LLC)
DrugClass IReported September 2, 2026 · Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.