Recalls in January 2026 (page 3)
471 recalls.
- Mung Beans packaged in 4lb polybags recall (LUBNA QUALITY PRODUCTS INC.)
FoodClass IIIReported March 4, 2026 · Presence of Thiamethoxam-PESTICIDE - Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz recall (J2C Hawaii LLC)
FoodClass IIReported March 4, 2026 · Ingredients List declares peanut but the Contains statement does not declare peanut - Gerber Arrowroot Biscuits recall (Gerber Products Company dba Nestle Infant Nutrition)
FoodClass IIReported March 4, 2026 · Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft... - Octopus Nuvo Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported March 4, 2026 · During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the... - Adapt Pump recall (Agiliti Health - Ellis)
Medical deviceClass IIReported March 4, 2026 · Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate... - Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167 recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Convenience kits used for dialysis maintenance Medline ADD A CATH DIALYSIS KIT SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746 recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline Kits containing Tego Connectors: Medline IR Pack recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - PIE PAK Models: P2HC-A recall (Edermy LLC)
Medical deviceClass IIReported March 4, 2026 · Lack of 510K clearance - PIE Trolley System Model: 2005 recall (Edermy LLC)
Medical deviceClass IIReported March 4, 2026 · Lack of 510K clearance - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Meijer STERILE saline wound wash recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) NAIL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) NAIL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Sterile Saline Wound Wash recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - The Tuna Salad product container is mislabeled with a Chicken Salad lid recall (Reser's Fine Foods, Inc.)
FoodClass IReported February 25, 2026 · Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad. - Woodland Gourmet Arrowroot Flour item code H59EE86 recall (Woodland Foods LLC)
FoodClass IIReported February 25, 2026 · Possible presence of Foreign Material - Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the... recall (Art Monkey LLC dba Why Not Natural)
FoodClass IReported February 25, 2026 · Potential to be contaminated with Salmonella - MOLLI 2 System System includes: MM1000 recall (Stryker Corporation)
Medical deviceClass IIReported February 25, 2026 · Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target... - Medline Surgical Packs: 1) PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Gowns: 1) GOWN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Drapes: 1) SHEET recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ARTHROSCOPY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT UROLOGY SLING recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ROBOTIC GYN CDS-1 recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OB KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) NEURO SHUNT- CODMAN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHEST/BREAST-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ADMIT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PPE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT GENERAL CLOSURE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BURN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) WMC I D PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT ACES INSERT PEG recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) TOTE ABRAMS KNEE ARTHROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LITHOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DENTAL PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC LINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OR ARTERIOGRAM recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ENDO KIT W/SYRINGE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SCC RF PAIN MGMT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANCILLARY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - MONARCH Platform recall (Auris Health, Inc)
Medical deviceClass IIReported February 25, 2026 · Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope... - Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported February 25, 2026 · Pumps were released without full testing being performed, including occlusion alarm testing. - Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot recall (TKS Co-pack Manufacturing, LLC)
FoodClass IIReported February 18, 2026 · Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. - Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot recall (TKS Co-pack Manufacturing, LLC)
FoodClass IIReported February 18, 2026 · Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. - Karison brand PANJIRI recall (Karison Foods & Snacks, Inc.)
FoodClass IIReported February 18, 2026 · Product contains milk, which is undeclared in the ingredient statement. - Karison brand ALSI PINNI recall (Karison Foods & Snacks, Inc.)
FoodClass IIReported February 18, 2026 · Product contains milk, which is undeclared in the ingredient statement. - Karison brand NO SUGAR ADDED BESAN LADDOO recall (Karison Foods & Snacks, Inc.)
FoodClass IIReported February 18, 2026 · Product contains milk, which is undeclared in the ingredient statement. - Karison brand PUNJABI PINNI recall (Karison Foods & Snacks, Inc.)
FoodClass IIReported February 18, 2026 · Product contains milk, which is undeclared in the ingredient statement. - Karison brand BESAN LADDOO recall (Karison Foods & Snacks, Inc.)
FoodClass IIReported February 18, 2026 · Product contains milk, which is undeclared in the ingredient statement. - Crunchy Caramel artisan dark chocolate with crunch brown sugar caramel pieces 60% Cacao recall (Cacao Art)
FoodClass IIReported February 18, 2026 · Undeclared allergen - milk. Product contains butter; cream is listed as a sub-ingredient of the butter, but milk is not declared in the ingredients or a... - Sodexo Stars Saccharin recall (Domino Foods Inc)
FoodClass IIIReported February 18, 2026 · Undeclared Aspartame - Brand: Red Button Movie House Popcorn Pack Size: 24 oz. / 680g. SKU/ recall (Lee's Commissary)
FoodClass IIReported February 18, 2026 · Product may contain foreign material. - Spicy Breakfast Burrito in a flour tortilla. Net Weight 10 oz recall (MG Foods-Compass Group)
FoodClass IIReported February 18, 2026 · foreign material (small hard plastic fragments) - Smoked Grouper Dip 7lb plastic tub with tamper proof lid 1/7lb tub per case. Keep... recall (ISLAND CRAB CORPORATION)
FoodClass IIReported February 18, 2026 · Undeclared Milk, Eggs, Sodium metabisulfite - Sonic Tots recall (McCain Foods USA Inc)
FoodClass IIReported February 18, 2026 · Foreign material (small hard plastic fragments). - Ore-Ida Tater Tots shaped potatoes recall (McCain Foods USA Inc)
FoodClass IIReported February 18, 2026 · Foreign material (small hard plastic fragments). - Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. recall (Costco Wholesale Corporation)
FoodClass IReported February 18, 2026 · Undeclared hazelnut. - a.) Preema brand Bright Red Food Colour Powder recall (KPCM New York Inc.)
FoodClass IIReported February 18, 2026 · Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40 - Carrot Top Kitchens Lime Ginger Hummus recall (Carrot Top Kitchens LLC)
FoodClass IReported February 18, 2026 · Contains undeclared sesame - Carrot Top Kitchens Cherry Pepper Hummus recall (Carrot Top Kitchens LLC)
FoodClass IReported February 18, 2026 · Contains undeclared sesame - Carrot Top Kitchens White Truffle Hummus recall (Carrot Top Kitchens LLC)
FoodClass IReported February 18, 2026 · Contains undeclared sesame - Carrot Top Kitchens Sundried Tomato and Caper Hummus recall (Carrot Top Kitchens LLC)
FoodClass IReported February 18, 2026 · Contains undeclared sesame - Carrot Top Kitchens Lemon & Garlic Hummus recall (Carrot Top Kitchens LLC)
FoodClass IReported February 18, 2026 · Contains undeclared sesame - UDENYCA recall (McKesson)
DrugClass IReported February 18, 2026 · Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the... - Oxycodone Hydrochloride Tablets recall (Amerisource Health Services LLC)
DrugClass IIReported February 18, 2026 · Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities. - Testosterone 100mg Anastrozole 4mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 87.5mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter