Recalls in Connecticut (page 3)
3932 recalls.
- Techno-Path Multichem AE Unassayed Level 3 recall (TECHNO-PATH MANUFACTURING LTD.)
Medical deviceClass IIReported October 28, 2026 · A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.... - Techno-Path Multichem AE Unassayed Level 2 REF: AE622X recall (TECHNO-PATH MANUFACTURING LTD.)
Medical deviceClass IIReported October 28, 2026 · A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.... - Techno-Path Multichem AE Unassayed Level 1 REF:AE621X recall (TECHNO-PATH MANUFACTURING LTD.)
Medical deviceClass IIReported October 28, 2026 · A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.... - 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... - Brand Name: VACUETTE Product Name: LH Lithium Heparin Separator Model/Catalog... recall (Greiner Bio-One North America, Inc.)
Medical deviceClass IIReported October 28, 2026 · Lot B26043FM may include EDTA contamination which introduces potassium while chelating calcium in patient samples, leading to falsely elevated potassium (K+)... - 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. - Think Surgical Square Driver REF: 109126 recall (Think Surgical, Inc.)
Medical deviceClass IIReported October 28, 2026 · Robotic system square drive failed to meet design specifications potentially resulting in pin becoming stuck in square driver or the pin wobbling during... - 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). - 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... - BAMAMON Recalls LED Projecting Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 22, 2026 · None reported. - Lithonia Lighting Recalls RSX Luminaires with Adjustable Tilt Arm Mountings Due to Risk of Serious Injury from Impact Hazard
Consumer productReported October 22, 2026 · The knuckle of the recalled adjustable tilt arm mountings can fail, allowing the luminaire to fall from the mounting arm, posing a risk of serious injury due... - Costway Recalls Convertible High Chairs Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for High Chairs
Consumer productReported October 22, 2026 · The convertible high chairs violate the mandatory safety standard for high chairs because they do not contain a passive restraint system and a child can slip... - VQQQ Gas Patio Heaters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported October 22, 2026 · Components on the recalled patio heaters can malfunction, causing gas to be released, posing a risk of serious injury or death from fire and burn hazards. - FoShanShiNanHaiQuNuoAiTongZhuangShangHang Recalls CIYTI Light-Up Princess Costumes Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 22, 2026 · The costumes violate the mandatory safety standard for toys because the button cell batteries can be accessed easily by children, posing a deadly ingestion... - The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists recall (Radiometer Medical ApS)
Medical deviceClass IIReported October 21, 2026 · In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood... - IQ200 SPRINT recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - DxU 840m Iris recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - 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... - Generic Name: BioFire¿ Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel ... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - 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. - Metoclopramide Tablets recall (American Health Packaging)
DrugClass IIReported October 21, 2026 · Presence of Foreign Tablets/Capsules - 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. - Hydrocortisone Sodium Succinate for Injection recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported October 21, 2026 · Failed Impurities/Degradation Specifications. - 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. - Convenience Kits containing CONMED AirSeal Access Ports KIT ROBOTICS UROLOGY... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC ... recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during... - 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... - 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... - MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control recall (Microgenics Corporation)
Medical deviceClass IIReported October 21, 2026 · Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone... - 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... - 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... - iFuse TORQ Implant System Model/Catalog Number: 10055T recall (SI-BONE, Inc.)
Medical deviceClass IIReported October 21, 2026 · The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. - Power F2 Powered Fastening System recall (Ferno-Washington Inc)
Medical deviceClass IIReported October 21, 2026 · Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system... - Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack recall (Sarnova HC, Llc)
Medical deviceClass IIReported October 21, 2026 · Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. - 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... - NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number... recall (Neuronetics, Inc.)
Medical deviceClass IIReported October 21, 2026 · Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly. - Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number:... recall (Cadwell Industries Inc)
Medical deviceClass IIReported October 21, 2026 · Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the... - BD Phoenix Panel NMIC-306. Catalog Number: 449292. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - BD Phoenix Panel NMIC-312. Catalog Number: 449082. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to... - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related... - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - usOpal Recalls Xalirium Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported October 15, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - Primark Recalls 101 Dalmatians Faux Leather Children’s Coin Purses Due to Phthalate Levels and Risk of Ingestion
Consumer productReported October 15, 2026 · The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through... - Papablic, of USA Recalls Convertible Bedside Sleepers Due to Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards
Consumer productReported October 15, 2026 · The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby... - Loving Thyself Rocks Recalls Crystal Glass Cups Due to Risk of Serious Injury from Ingestion and Laceration Hazards
Consumer productReported October 15, 2026 · Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards. - HatsanUSA Recalls Blitz Air Rifles Due to Risk of Serious Injury or Death from Projectile Hazard
Consumer productReported October 15, 2026 · The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from... - 3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported October 15, 2026 · The recalled thermal laminators can overheat, posing a fire hazard. - Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station recall (Nihon Kohden America LLC)
Medical deviceClass IIReported October 14, 2026 · Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized... - Battle Bandage recall (Safeguard US Operating LLC)
Medical deviceClass IIReported October 14, 2026 · Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and... - Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product... recall (SWEET SENSI)
FoodClass IIReported October 14, 2026 · Staphylococcus aureus detected in product. - 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. - 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 - Berlin Seeds Alfalfa Sprouting Seeds recall (Berlin Seeds)
FoodClass IReported October 14, 2026 · Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination. - Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5... recall (The Better Bakehouse Snack Company)
FoodClass IReported October 14, 2026 · Undeclared Milk.