Recalls in February 2026 (page 3)
364 recalls.
- Great Value Cottage Cheese Small Curd 4% Milkfat recall (SAPUTO CHEESE USA, INC)
FoodClass IIReported March 25, 2026 · Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products... - Great Value Lowfat Cottage Cheese Small Curd 2% Milkfat recall (SAPUTO CHEESE USA, INC)
FoodClass IIReported March 25, 2026 · Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products... - Great Value Fat Free Cottage Cheese Small Curd 0% Milkfat recall (SAPUTO CHEESE USA, INC)
FoodClass IIReported March 25, 2026 · Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products... - CLOVER SONOMA SOUR CREAM recall (SAPUTO CHEESE USA, INC)
FoodClass IIReported March 25, 2026 · Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products... - CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT recall (SAPUTO CHEESE USA, INC)
FoodClass IIReported March 25, 2026 · Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products... - GREENWAY FARMS of Georgia JALAPENO DILL PICKLES CHIPS Net Wt 16 fl oz recall (BlueFrog Foods)
FoodClass IIReported March 25, 2026 · No process authority - GREENWAY FARMS of Georgia GARLIC DILL PICKLES CHIPS Net Wt 16 fl oz recall (BlueFrog Foods)
FoodClass IIReported March 25, 2026 · No process authority - Dreamland's Zaatar Chickpea Salad is packaged in poly bags with a generic label which... recall (Dreamland Inc)
FoodClass IReported March 25, 2026 · Undeclared Sesame, Soy, Wheat - Butter Powder recall (Bluegrass Ingredients Inc.)
FoodClass IReported March 25, 2026 · Positive Salmonella contamination - Butter-Rich Powder recall (Bluegrass Ingredients Inc.)
FoodClass IReported March 25, 2026 · Potential Salmonella contamination - Dexamethasone Sodium Phosphate Injection recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIReported March 25, 2026 · Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs... - Pitavastatin Tablets recall (Annora Pharma Private Limited)
DrugClass IIIReported March 25, 2026 · Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg - Battery Charging Station recall (Datascope Corp.)
Medical deviceClass IIIReported March 25, 2026 · The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to ... - Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number:... recall (Hologic, Inc.)
Medical deviceClass IIReported March 25, 2026 · Due to product exhibiting potential to generate either invalid or false negative results. - Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number:... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported March 25, 2026 · After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion ... recall (Elekta, Inc.)
Medical deviceClass IIReported March 25, 2026 · Due to adapter not being properly aligned or locked in place. - Cub Pediatric Crib recall (Stryker Medical Division of Stryker Corporation)
Medical deviceClass IIReported March 25, 2026 · Cribs sold in the USA are missing two access door warning labels. - Artegraft Vascular Graft recall (LeMaitre Vascular, Inc.)
Medical deviceClass IIReported March 25, 2026 · Labeling mix-up resulting in the incorrect lot outer packaging of product. - Brand Name: Welch Allyn recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported March 25, 2026 · Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible... - MICS3 Angled Sagittal Saw Attachment recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported March 25, 2026 · A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the... - Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software... recall (Abbott Diagnostics Scarborough, Inc.)
Medical deviceClass IIReported March 25, 2026 · It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use. - House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream recall (House Of Flavors, Inc.)
FoodClass IReported March 18, 2026 · Undeclared egg - Made Fresh Salads brand Tofu Whipped recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Whipped Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Walnut Raisin Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Vegetable Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Sundried Tomato Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Strawberry Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Scallion Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Lox Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Jalapeno Cheddar Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Jalapeno Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Garlic & Herb Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Blueberry Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Caramel Apple Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Made Fresh Salads brand Apple Cinnamon Cream Cheese recall (Made Fresh Salads Inc)
FoodClass IReported March 18, 2026 · Products may be contaminated with Listeria monocytogenes. - Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream recall (Cocos Wholesale and Imports, LLC)
FoodClass IIReported March 18, 2026 · Label lists flour as a sub-ingredient of the shells, and ricotta cheese as a sub-ingredient of the cream but does not declare wheat or milk. - Coco's Italian Market Heat-n-Eat Fettuccini Alfredo in homemade Alfredo Sauce recall (Cocos Wholesale and Imports, LLC)
FoodClass IIReported March 18, 2026 · Label lists semolina and durum flour as sub-ingredients of the pasta, but does not declare wheat - Lowes Foods sour cream and onion flavored potato chips recall (Uncle Ray's LLC)
FoodClass IIReported March 18, 2026 · Inaccurate nutritional data in Nutrition Facts including but not limited to, understated sodium content. Undeclared ingredients including but not limited to... - Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES recall (Willamette Valley Pie Company, LLC)
FoodClass IIReported March 18, 2026 · Potential contamination with listeria monocytogenes. - Frozen Raw Bulk 8 inch Blueberry Crumble Pie recall (Willamette Valley Pie Company, LLC)
FoodClass IIReported March 18, 2026 · Potential contamination with listeria monocytogenes. - Hortex Mieszanka 9 - skBadnikowa Spring vegetable mix with 9 ingredients recall (Polski Ogrod Sp. z o.o.)
FoodClass IIReported March 18, 2026 · potential contamination with glass - Rosabella brand MORINGA recall (Ambrosia Brands LLC)
FoodClass IReported March 18, 2026 · Product may be contaminated with Salmonella - C2O Coconut Water with Pulp recall (Tipp Distributors, Inc. dba Novamex)
FoodClass IIIReported March 18, 2026 · The outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar (5g per... - Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor recall (International Life Sciences)
Medical deviceClass IIReported March 18, 2026 · Augmentation devices failed bacterial endotoxin testing. - Artelon FlexBand Plus Ref: 41054 & 41057 recall (International Life Sciences)
Medical deviceClass IIReported March 18, 2026 · Augmentation devices failed bacterial endotoxin testing. - Artelon FlexBand Dynamic Matrix Ref: 31057 recall (International Life Sciences)
Medical deviceClass IIReported March 18, 2026 · Augmentation devices failed bacterial endotoxin testing. - EndoVive Safety PEG Kit recall (Boston Scientific Corporation)
Medical deviceClass IIReported March 18, 2026 · Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog... recall (Exactech, Inc.)
Medical deviceClass IIReported March 18, 2026 · Impactor handle may be missing cross-pin - Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog... recall (Exactech, Inc.)
Medical deviceClass IIReported March 18, 2026 · Impactor handle may be missing cross-pin - IBA Proton Therapy System - PROTEUS 235 recall (Ion Beam Applications S.A.)
Medical deviceClass IIReported March 18, 2026 · It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS... - Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat recall (Perfect Pasta, Incorporated)
FoodClass IReported March 11, 2026 · Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy. - tippy toes apple pear banana 6 months & up baby food 2-4OZ recall (IF Holding II, LLC)
FoodClass IIReported March 11, 2026 · Potential contamination with patulin. - Junebar Chocolate Cherry All Natural Snack Bar recall (Juniper Granola, LLC)
FoodClass IReported March 11, 2026 · Products contain undeclared milk and soy. - Junebar Peanut Chocolate Chip All Natural Snack Bar recall (Juniper Granola, LLC)
FoodClass IReported March 11, 2026 · Products contain undeclared milk and soy. - VERGANI 1944 MILANO 'PANDORO CLASSICO' Gluten Free recall (Italianway Import, Inc.)
FoodClass IIReported March 11, 2026 · Potential contamination with foreign material (Teflon fragments) from flaking cooking molds. - Amnesteem recall (MYLAN PHARMACEUTICALS INC)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Tirzepatide Inj recall (New Life Pharma LLC)
DrugClass IIReported March 11, 2026 · Lack of Assurance of Sterility - Tirzepatide Inj recall (New Life Pharma LLC)
DrugClass IIReported March 11, 2026 · Lack of Assurance of Sterility - Semaglutide Inj. recall (New Life Pharma LLC)
DrugClass IIReported March 11, 2026 · Lack of Assurance of Sterility - Semaglutide Inj recall (New Life Pharma LLC)
DrugClass IIReported March 11, 2026 · Lack of Assurance of Sterility - MAXIMUM recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - MAXIMUM recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - FIVE-STAR recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - Midodrine Hydrochloride Tablets recall (The Harvard Drug Group LLC)
DrugClass IIReported March 11, 2026 · Defective container; inadequately sealed blister packaging. - Nilotinib Capsules recall (Cipla USA, Inc.)
DrugClass IIIReported March 11, 2026 · Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection... - Nilotinib Capsules recall (Cipla USA, Inc.)
DrugClass IIIReported March 11, 2026 · Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection... - Semaglutide recall (Harbin Jixianglong Biotech Co., Ltd.)
DrugClass IIReported March 11, 2026 · CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution - Semaglutide recall (Harbin Jixianglong Biotech Co., Ltd.)
DrugClass IIReported March 11, 2026 · CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution - Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S ... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported March 11, 2026 · The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values. - Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 ... recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: B. Braun Product Name: 21GA WINGED INFUSION recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF ... recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Wellsley Farms Farm- Raised Atlantic Salmon Net WT. 32 oz. recall (SLADE GORTON & CO., INC.)
FoodClass IIReported March 4, 2026 · Contaminated with Listeria monocytogenes - Valley Springs Steamed Distilled Water. 1 Gal Net recall (Valley Springs Artesian Gold, LLC)
FoodClass IIReported March 4, 2026 · Water was bottled under insanitary conditions. - Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net recall (Valley Springs Artesian Gold, LLC)
FoodClass IIReported March 4, 2026 · Water was bottled under insanitary conditions. - Valley Springs 100% Natural Bottled Water packaged in the following size plastic jug... recall (Valley Springs Artesian Gold, LLC)
FoodClass IIReported March 4, 2026 · Water was bottled under insanitary conditions. - IQF frozen Blueberry recall (Oregon Potato Company LLC)
FoodClass IReported March 4, 2026 · Listeria monocytogenes - Prime Food Processing Dried Croaker Fish recall (Prime Food Processing LLC.)
FoodClass IReported March 4, 2026 · Uneviscerated Fish - Eptifibatide Injection recall (Slate Run Pharmaceuticals)
DrugClass IIIReported March 4, 2026 · Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved... - Amantadine HCl recall (AvKARE)
DrugClass IIReported March 4, 2026 · Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution. - Adbry recall (LEO PHARMA INC)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber. - Campy CVA Medium 100/PK recall (Remel, Inc)
Medical deviceClass IIReported March 4, 2026 · Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium. - Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR recall (Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha)
Medical deviceClass IIReported March 4, 2026 · Software anomaly in the patient positioning system may result in positional discrepancy. - Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR recall (Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha)
Medical deviceClass IIReported March 4, 2026 · Software anomaly in the patient positioning system may result in positional discrepancy. - Evajoy Above-Ground Pools 48 Inches and Taller Recalled Due to Drowning Hazard; Manufactured by Shenzhen Danya Tech
Consumer productReported February 27, 2026 · The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk. - Babysense Max View Baby Monitors Recalled Due to Fire Hazard; Manufactured by Hisense
Consumer productReported February 27, 2026 · The display or "parent" unit of the Max View baby monitors can overheat and/or spark when charging, posing a fire hazard to consumers. - Andersen Windows Recalls Window Opening Control Devices Sold as Kits or Installed on 100 Series Casement Windows Due to Fall and Serious Injury Hazards
Consumer productReported February 27, 2026 · The window opening control devices can break or detach after accidental or other impact, allowing the window to be opened, posing fall and serious injury... - SumDirect LED Mini Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported February 27, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell... - Todson Recalls Concord Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported February 27, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system and positional... - Joyreal Busy Board Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking and Laceration Hazards; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Indream Store
Consumer productReported February 27, 2026 · The recalled children's toys violate the small parts ban because the small mirror can detach from the toy, posing a deadly choking hazard. In addition, the... - Zelbuck Children's Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by n b plus
Consumer productReported February 27, 2026 · The recalled children's chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When... - TheKiddoSpace Recalls Children's Sensory Swing Due to Risk of Serious Injury or Death from Strangulation
Consumer productReported February 27, 2026 · The recalled swing's flexible fabric can form loops that can entangle a child's head or neck, posing a risk of serious injury or death from strangulations.