Recalls in May 2026 (page 3)
579 recalls.
- Medline Convenience Kits: 1) DYNJ905503F recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net... recall (Dkiru LLC)
FoodClass IIReported June 24, 2026 · Undeclared melatonin. - Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50 recall (International Food Products Corporation)
FoodClass IIReported June 24, 2026 · Potential for Salmonella - Dairy House Ingredient Systems Vanilla Dairy Powder recall (International Food Products Corporation)
FoodClass IIReported June 24, 2026 · Potential for Salmonella - Legacy Tex Dressing Stabilizer Blend #7604-50 recall (International Food Products Corporation)
FoodClass IIReported June 24, 2026 · Product tested positive for Salmonella - azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT... recall (Azuma Foods International Inc USA)
FoodClass IReported June 24, 2026 · Undeclared fish. - White Cheddar Seasoning packed in the following sizes and configurations: 1. Net... recall (Jonco Industries)
FoodClass IReported June 24, 2026 · Products were made with recalled California Dairies milk powder due to Salmonella. - Salt recall (United Salt Corp)
FoodClass IIIReported June 24, 2026 · Plain salt was labeled as iodized and iodized salt was labeled as plain. - Fairhope Roasting Company Cold Brew Coffee Concentrate recall (Fairhope Roasting Company)
FoodClass IIReported June 24, 2026 · Product requires refrigeration but the label is missing a "Keep Refrigerated" statement - Great Value Hawaiian Roll 4pk recall (United States Bakery)
FoodClass IIReported June 24, 2026 · Firm observed oily and sticky substance on direct food contact surface packaging of finished product. - Nutrisystem recall (Nutrisystem Inc)
FoodClass IIReported June 24, 2026 · Undeclared Allergen (Soy) - .155 CRUNCHY CANNOLI GLUTEN FREE intended use: DESSERT condition: shelf stable shelf... recall (MID DOLCIARIA SRL)
FoodClass IIReported June 24, 2026 · The product contains unapproved colors chlorophyll E140 and E141. - CANNOLI SICILIANI intended use: DESSERT condition: shelf stable shelf life: 12 month... recall (MID DOLCIARIA SRL)
FoodClass IIReported June 24, 2026 · The product contains unapproved colors chlorophyll E140 and E141. - safco SensiCaine-Ultra recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - PureLife recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Dental City TOPICAL ANESTHETIC GEL recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Burkhart topical anesthetic gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - DHP Topical Anesthetic Gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Quala Dental Products recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Pearson Quality Topical Anesthetic Gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Aripiprazole Tablets USP recall (Ajanta Pharma USA Inc)
DrugClass IIReported June 24, 2026 · Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg. - Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride recall (IntegraDose Compounding Services LLC)
DrugClass IIReported June 24, 2026 · Subpotent Drug - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - Alyacen 7/7/7 recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported June 24, 2026 · Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities. - Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog... recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 ... recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported June 24, 2026 · Due to unsealed portions of pouches. - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta"... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported June 24, 2026 · Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening... - MEDLINE Medical Procedure Kits labeled as: 1) CRANI recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) RETINA LAC/USC CDS recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: KIT URO ROBOT CYSTECTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BASIC GYN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CAROTID NEURO PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: NURSING KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: DR FERNANDEZ recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CV DRAPING/BASIN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: TONSIL PACK CATH recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CHEST EXPLORATION ECMO recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: CATH 22F ROBINSON STRL 5'S PK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ORAL RESTORATION recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BNT CV PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CH OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: LAPAROSCOPY COMBINED - NO NDL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheterization Tray and Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Pre-connected Urethral Catheterization Tray and Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheterization Tray recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheter recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - Giraffe OmniBed Field Replaceable Unit recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - Giraffe OmniBed recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported June 24, 2026 · Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot... - TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported June 24, 2026 · Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot... - Ritmed Neurological Sponges recall (AMD Medicom Inc.)
Medical deviceClass IIReported June 24, 2026 · Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not... - Ritmed Neurological Sponges recall (AMD Medicom Inc.)
Medical deviceClass IIReported June 24, 2026 · Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not... - Impella CP Set with SmartAssist. Product Codes: 1000080 recall (Abiomed, Inc.)
Medical deviceClass IReported June 24, 2026 · Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical... - Medtronic O-arm O2 Imaging System. Model Number: BI70002000. recall (Medtronic Navigation, Inc.-Boxborough)
Medical deviceClass IIReported June 24, 2026 · Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware. - ALYON Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. - Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 24, 2026 · Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended ... - Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 24, 2026 · Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended ... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 24, 2026 · Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices. - Panda Freestanding Warmer recall (Datex-Ohmeda Inc)
Medical deviceClass IReported June 24, 2026 · Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the... - Giraffe Warmer with Integrated Resuscitation System recall (Datex-Ohmeda Inc)
Medical deviceClass IReported June 24, 2026 · Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the... - Giraffe Stand-alone Infant Resuscitation System recall (Datex-Ohmeda Inc)
Medical deviceClass IReported June 24, 2026 · Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the... - NEURO NOURISH dietary supplement recall (SENSORY SUPPLEMENT LLC)
FoodClass IIReported June 17, 2026 · Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste. - DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz recall (U.S. Tov, Inc. dba U.S. Trading Company)
FoodClass IIReported June 17, 2026 · Potential contamination with lead. - 1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules recall (Total Nutrition Inc)
FoodClass IReported June 17, 2026 · Product may be contaminated with Salmonella. - Individual Unit Label recall (Kettle Cuisine, LLC)
FoodClass IReported June 17, 2026 · Contains undeclared allergen (shrimp). - HH Fresh Trading Corp. recall (HH FRESH TRADING CORP)
FoodClass IReported June 17, 2026 · Imported Enoki Mushrooms tested positive for Listeria Monocytogenes. - ESTRELLA recall (Refresqueria Estrella Inc.)
FoodClass IIIReported June 17, 2026 · Undeclared FD&C Red 40 - Farm Rich Pizza Cheese Crunchers recall (Rich Products Corp)
FoodClass IIReported June 17, 2026 · May contain metal pieces