Recalls in September 2026 (page 2)
322 recalls.
- Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Direxion Torqueable Microcatheter recall (Boston Scientific Cork, Ltd.)
Medical deviceClass IIReported October 28, 2026 · The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the... - Generic Name: Softmed Breathables Advanced Toric recall (CooperVision, Inc.)
Medical deviceClass IIReported October 28, 2026 · The affected products bear an incorrect statement on the carton packaging indicating that the product is "Indicated for Extended Wear". However, this product... - CareLink Clinic recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported October 28, 2026 · CareLink Clinic software version 4.4A includes a software defect in the Settings Calculator feature in which the calculation logic fails to use custom values... - ROTOR ASSY-SW41 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 28, 2026 · Rotors have been found with a non-conforming microstructure, which may result in some rotors breaking into two or more pieces during use. Rotors that break... - ROTOR ASSY-SW40 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 28, 2026 · Optima XE XPN ultracentrifuge rotors may contain a microstructure defect that can cause rotors to break into two or more pieces (bifurcate) during a... - Philips Smart-hopping 2.0 AP 1.4 GHz recall (Philips North America)
Medical deviceClass IIReported October 28, 2026 · Unreliable wireless roaming behavior of Smart-hopping 1.0 wireless clients during transport when connecting to Smart-hopping 2.0 infrastructure, resulting in... - B Braun SAFSITE Injection Site recall (B Braun Medical Inc)
Medical deviceClass IIReported October 28, 2026 · Potential for leakage and backflow at the Safsite valve. - Amplatzer Amulet Left Atrial Appendage Occluder Model Numbers 1. 9-ACP2-007-016 ... recall (Abbott)
Medical deviceClass IIReported October 28, 2026 · Changes to Instructions for Use (IFU) for the device regarding risk of Pulmonary Artery Injury (PAI). - Philips Lumify Diagnostic Ultrasound System recall (Philips Ultrasound, LLC)
Medical deviceClass IReported October 28, 2026 · Ultrasound system may: 1) Not recognize previous transducer registration, prevent scanning, require re-registration with Wi-Fi/cellular access, which may be... - V*Home recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - V+ Pro Emergency recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC Model Number: PRT-01098-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - V+Pro Model Number: PRT-01185-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VCSN+Pro Model Number: PRT-01184-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN Model Number: PRT-01100-000 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC+Pro recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VC+Pro Model Number: PRT-00900-001 recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN+Pro recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - VOCSN+Pro recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported October 28, 2026 · Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of... - Deano's Pasta recall (DEANO'S PASTA)
FoodClass IReported October 21, 2026 · Undeclared Lobster - Made From Plants recall (DARING FOODS INC)
FoodClass IIReported October 21, 2026 · defective packaging; packaging can rupture/explode during cooking. - J. HIGGS Loaded Bacon & Cheddar Potato Chips recall (Saratoga Potato Chips LLC)
FoodClass IIReported October 21, 2026 · Undeclared soy. - Holsum Spinach Flour Tortillas Large recall (Holsum De Puerto Rico, Inc.)
FoodClass IIReported October 21, 2026 · Undeclared colors (FD&C Blue No. 1 and FD&C Yellow No. 5) - Sermorelin recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of process control - Tirzepatide/Niacinamide 2mL vial recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of assurance of sterility. - Metoclopramide Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported October 21, 2026 · Presence of Foreign Tablets/Capsules - Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Discrepancy in the shelf-life of a component - Vinyl Instrument Guards recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported October 21, 2026 · Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated. - IntelePACS recall (INTELERAD MEDICAL SYSTEMS INCORPORATED)
Medical deviceClass IIReported October 21, 2026 · Following a Chromium-based web-browser, report and displayed images may not match. - Medline surgical convenience kits labeled as: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) CV BASIN PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) EAR recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: VEIN HARVESTING PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - 1) Product Name AUD OPEN HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: CABG AUXILIARY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - TS Misc. Instruments Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Femoral Prep Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Universal Baseplate Finishing Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Williams Cystoscopic Injection Needles recall (Cook Incorporated)
Medical deviceClass IIReported October 21, 2026 · The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during... - LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762. recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIIReported October 21, 2026 · In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct... - Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported October 21, 2026 · The potential for the devices to be mislabeled with the incorrect length. - REF: P65 ST862 CoLag SCREW recall (In2bones USA, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws. - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture recall (Ethicon, LLC)
Medical deviceClass IIReported October 21, 2026 · Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that... - Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported October 21, 2026 · Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift... - FORWARD Gunshot Wound Kit recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported October 21, 2026 · Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the... - NaviFlex LW Pusher recall (Boston Scientific Corporation)
Medical deviceClass IIReported October 21, 2026 · Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this... - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - SIERRA NEVADA CHEESE GRAZIERS RAW MILK SHARP CHEDDAR recall (Sierra Nevada Cheese Company, Inc)
FoodNot Yet ClassifiedReported October 14, 2026 · Potential contamination due to E. coli O26:H11. - Croissant recall (J K Patisserie & Bakery LLC)
FoodClass IIReported October 14, 2026 · Egg was not declared in the Contains statement. - Chocolate Chip Cookies packaged in a cardboard box recall (J K Patisserie & Bakery LLC)
FoodClass IIReported October 14, 2026 · Soy was not declared in the Contains statement. - Lemon Blueberry Loaf packaged in a cardboard box recall (J K Patisserie & Bakery LLC)
FoodClass IIReported October 14, 2026 · Product contains undeclared soybean oil and soy lecithin in the Ingredient Statement. Soy was not declared in the Contains statement. - biQ-FEL recall (A&P CREATIONS)
FoodClass IReported October 14, 2026 · Product contains undeclared Sildenafil and Tadalafil. - X10 Natural Enhancement Supplement recall (A&P CREATIONS)
FoodClass IReported October 14, 2026 · Product contains undeclared Sildenafil and Tadalafil. - QUESO PALMITA. Generic Name: Pastel de Queso recall (QUESO PALMITA GP LLC)
FoodClass IIReported October 14, 2026 · Undeclared milk, cheese declared - Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black... recall (GIAS FOOD INC.)
FoodClass IReported October 14, 2026 · Contamination with Listeria monocytogenes