Recalls in Maine (page 4)
3867 recalls.
- Tretinoin Cream USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported October 14, 2026 · Failed Impurities/Degradation Specifications - Tretinoin Cream USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported October 14, 2026 · Failed Impurities/Degradation Specifications - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 85/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 76/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 64/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE/CYANOCOBALAMIN 26/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - SEMAGLUTIDE/CYANOCOBALAMIN 9/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - QUAD-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to processing equipment used in compounded product. - SERMORELIN ACETATE 1 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - SEMAGLUTIDE/CYANOCOBALAMIN 3/2 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - SEMAGLUTIDE 3 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - TIRZEPATIDE 26 MG/ML INJECTABLE recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - Fosfomycin Tromethamine Granules for Oral Solution recall (Cipla USA, Inc.)
DrugClass IIReported October 14, 2026 · Failed Impurities/Degradation Specifications - Lidocaine Ointment USP recall (Preferred Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Failed Content Uniformity Specifications - Sterile High Performance Ultra Lubricating Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile Eye Drops Redness Relief recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile Lubricant Dry Eye Relief Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Eye Drops MAXIMUM recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile EYE DROPS Advanced Relief recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Sterile EYE DROPS AC recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Artificial Tears Sterile Lubricant Eye Drops recall (K.C. Pharmaceuticals, Inc.)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Intellijoint Navigation System: Workstation G2 Configured recall (Intellijoint Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro... - HexaVue Focus Integration System recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images... - TufTex¿ Over-the-Wire Embolectomy Catheter recall (LeMaitre Vascular, Inc.)
Medical deviceClass IIReported October 14, 2026 · Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing. - T1 Patient Monitor. Operator's Manual: T1 Patient Monitor recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneView Series. Operator's Manuals: T5 / T8 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama... recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80 recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22. recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM 12M/ePM 12MA/ ePM... recall (Mindray DS USA, Inc.)
Medical deviceClass IIIReported October 14, 2026 · Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions - Alphenix INFX-8000C/B5 recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported October 14, 2026 · Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and... - SEDIPLAST recall (POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC)
Medical deviceClass IIReported October 14, 2026 · During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube... - ABD HYSTERECTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - GYN LAPAROSCOPY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - MAJOR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - UROLOGY MAJOR recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - HEART PREP TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI LAP/GYN recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PLASTICS TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - LAPAROSCOPIC PROSTATECTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ROBOTIC PROSTATECTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PACK OPEN HEART CFH recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - CRANIOTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ENDOVASCULAR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ADULT HEART TRAY SHANDS JACKS recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - GYN LAPAROSCOPY/LAPAROTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI TRUCUSTOM BUNDLE recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog... recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported October 14, 2026 · Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed... - Rollator recall (Medline Industries, LP)
Medical deviceClass IIReported October 14, 2026 · The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator... - Rollator recall (Medline Industries, LP)
Medical deviceClass IIReported October 14, 2026 · The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator... - BARD EP XT DECAPOLAR STEERABLE recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported October 14, 2026 · Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to... - DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE recall (Beckman Coulter Inc.)
Medical deviceClass IIReported October 14, 2026 · Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical... - DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE recall (Beckman Coulter Inc.)
Medical deviceClass IIReported October 14, 2026 · Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical... - Sperm Ab ELISA recall (DRG International, Inc.)
Medical deviceClass IIReported October 14, 2026 · Potential for false negative patient results. - 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... - Glypto Device recall (Limitless Cryo Spa LLC)
Medical deviceClass IIReported October 14, 2026 · Lack of 510(k) clearance. - Spectral CT and Spectral CT 7500 RT recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported October 14, 2026 · Software issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or unintended... - HALYARD Laparoscopy Comprehensive Pack II REF: 49332 recall (GRI Medical & Electronic Technology Co., Ltd.)
Medical deviceClass IIReported October 14, 2026 · Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter - Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient... recall (QUANTUM OPS Inc)
Medical deviceClass IIReported October 14, 2026 · Due to a manufacturing issue (inadequate weld) for patient head positioning system. - VERIFY Biological Steam Test Pack Model/Catalog Number: S3069 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological Steam Test Pack Model/Catalog Number: S3065 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006 recall (Steris Corporation)
Medical deviceClass IIReported October 14, 2026 · Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization... - The Conqueror Recalls Avengers Medals Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets
Consumer productReported October 8, 2026 · The recalled medals violate the mandatory safety standard for magnets because the high-powered magnets may detach, posing a deadly ingestion hazard to... - Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks Due to Risk of Serious Injury or Death from Burn and Fire Hazards
Consumer productReported October 8, 2026 · The fireplace's lava rocks can ignite and explode when heated in the propane insert, posing a risk of serious injury or death from burn and fire hazards. - Romorgniz Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported October 8, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Pacearth Direct Recalls PACEARTH Swing Seats Due to Risk of Serious Injury from Fall Hazard
Consumer productReported October 8, 2026 · The seats, metal carabiners or quick links, or webbing straps of the recalled swing seats can break during use, posing a risk of serious injury due to fall... - ONTHEWEI Recalls Baby Bath Seats Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats
Consumer productReported October 8, 2026 · The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious... - Decathlon America Recalls Van Rysel GRVL AF Bicycles Due to Risk of Serious Injury or Death from Crash Hazard
Consumer productReported October 8, 2026 · The recalled bicycles' front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard. - DR Power Equipment Recalls Pilot and Premier Trimmer Mowers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported October 8, 2026 · Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards. - Giant Bicycle Recalls LED-Light Keys Included with SureLock Bike Lock Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported October 8, 2026 · The LED-light key that was included with certain SureLock Bicycle Lock sets violates the mandatory safety standard for consumer products with button cell and... - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Travel Air recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Impulsator recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - In-Line Valve recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - Intrapulmonary Percussive Ventilation recall (Percussionaire Corporation)
Medical deviceClass IIReported October 7, 2026 · Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter... - HeartSine samaritan PAD recall (HeartSine Technologies Ltd)
Medical deviceClass IIIReported October 7, 2026 · Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check. - Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 18" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 8" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 2 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 1 LINE recall (ASP Global, LLC.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct...