Recalls in Vermont (page 5)
3845 recalls.
- Todd's Seeds Sprouting Seed Mix - Broccoli recall (TODD'S SEEDS LLC)
FoodClass IReported October 7, 2026 · Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall) - Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccoli recall (TODD'S SEEDS LLC)
FoodClass IReported October 7, 2026 · Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall) - Todd's Seeds Alfalfa Sprouting Seeds recall (TODD'S SEEDS LLC)
FoodClass IReported October 7, 2026 · Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall) - Paroxetine Extended-Release Tablets recall (Apotex Corp.)
DrugClass IIReported October 7, 2026 · Failed dissolution specifications. - Buprenorphine Hydrochloride recall (Par Health USA, LLC)
DrugClass IIReported October 7, 2026 · Crystallization - Zoladex recall (TerSera Therapeutics LLC)
DrugClass IIReported October 7, 2026 · Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours. - Estradiol Gel recall (Amneal Pharmaceuticals, LLC)
DrugClass IIReported October 7, 2026 · Defective Container; packets were found to be either empty or partially full. - Ranolazine Extended-Release Tablets recall (Ajanta Pharma USA Inc)
DrugClass IIReported October 7, 2026 · Failed Dissolution Specifications: below specification - Atellica CH Revised C-Reactive Protein recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported October 7, 2026 · The potential for falsely elevated results. - CHARLOTTE CLAW Screw recall (Wright Medical Technology, Inc.)
Medical deviceClass IIReported October 7, 2026 · Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads... - HOPKINS Telescope 30¿ recall (Karl Storz Endoscopy)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect inside packaging label for eyepiece. - 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... - Brand Name: Penumbra System recall (Penumbra Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to manufacturing issues reperfusion catheters may fracture. - Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application recall (Tandem Diabetes Care, Inc.)
Medical deviceClass IIReported October 7, 2026 · A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application... - Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable. - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code:... recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter. - Evolution upgrade 1.5T amd Evolution upgrade 3.0T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Upgrade to MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Upgrade dStream recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - SmartPath to MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - SmartPath to dStream for 1.5T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - MR 5300 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Elition S and Ingenia Elition X. recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Ambition S and Ingenia Ambition X. recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia 3.0T and 3.0T CX recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia 1.5T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Blue Seal SE and Blue Seal XE recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I. recall (NOXBOX LTD)
Medical deviceClass IIReported October 7, 2026 · Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors. - Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 7, 2026 · Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the... - PALACOS MV pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS MV+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS R+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS R pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - 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... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800 recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number:... recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number:... recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - 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... - Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v recall (Volcano Corp)
Medical deviceClass IIReported October 7, 2026 · Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment. - 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) ... - Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED recall (Medline Industries, LP)
Medical deviceClass IReported October 7, 2026 · Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially... - Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories recall (Medline Industries, LP)
Medical deviceClass IReported October 7, 2026 · Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially... - Brand Name: Ferndale Laboratories recall (Custom Interventional Pain Management, LLC)
Medical deviceClass IIReported October 7, 2026 · Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits. - 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... - Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 26" DUAL BLADDER 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:DISPOSABLE TOURNIQUET CUFF 20" DUAL BLADDER 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:DISPOSABLE TOURNIQUET CUFF 20" DUAL BLADDER 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF 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: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF 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: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF 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: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF 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: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF 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: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF 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: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF 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: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF 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: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF 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...