Recalls in Illinois (page 5)
4177 recalls.
- 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... - 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. - Glypto Device recall (Limitless Cryo Spa LLC)
Medical deviceClass IIReported October 14, 2026 · Lack of 510(k) clearance. - 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... - Coco G's Courmet Flaming Cheddar Hots recall (Coco G's Snack Foods, Inc.)
FoodClass IReported October 7, 2026 · Potential Salmonella contamination. - Lior brand Cinnamon Ground Seasoning recall (Galil Importing Corp)
FoodClass IIReported October 7, 2026 · Product contains elevated levels of lead. - Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil recall (LMSI, LLC)
FoodClass IIReported October 7, 2026 · Product contains garlic essential oil not approved for culinary use - Benzoyl Peroxide Wash recall (SV Labs Toronto Corporation)
DrugClass IIReported October 7, 2026 · Microbial contamination of topical product. - Benzoyl Peroxide Wash recall (SV Labs Toronto Corporation)
DrugClass IIReported October 7, 2026 · Microbial contamination of topical product. - Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER... recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported October 7, 2026 · Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError... - 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... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Positron Emission Tomography and Computed Tomography System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - Computed Tomography X-ray System recall (Shanghai United Imaging Healthcare Co., Ltd.)
Medical deviceClass IIReported October 7, 2026 · Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are... - EnCor EnCompass Breast Biopsy and Tissue Removal System Console recall (Bard Peripheral Vascular Inc)
Medical deviceClass IIReported October 7, 2026 · Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2) ... - Fisher Scientific Sure-Vue Urine hCG recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - Fisher Scientific Sure-Vue Urine hCG Strip recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - Fisher Scientific Sure-Vue Serum/Urine hCG recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - McKesson CONSULT hCG Urine Cassette recall (Alere San Diego, Inc.)
Medical deviceClass IIReported October 7, 2026 · hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. - 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. - VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable... recall (Draeger, Inc.)
Medical deviceClass IReported October 7, 2026 · Potential cracks in the hose, which could lead to leakage or the hose falling off. - 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... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34" 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 34" 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 30" 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 30" 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 24" 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 24" 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 18" 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...