Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,541 recalls have been distributed to Vermont in the last 12 months.
Showing 3361–3380 of 47,027 recalls
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PCR Cartridges used with MAX System. Model Number: 437519 Recalled by...
The Issue: Potential for signal drift in specific lots of BD PCR Cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Recalled...
The Issue: The VITROS XT 7600 Integrated System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...
The Issue: The VITROS 5600 Integrated System software versions 3.8.0 may not correctly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System...
The Issue: The VITROS 3600 Immunodiagnostic System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bodor P and C series laser cutting machines Recalled by Jinan Bodor Cnc...
The Issue: Non-compliant laser products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Systane Lubricant Eye Drops Recalled by Alcon Research LLC Due to Non-Sterility
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colchicine Capsules 0.6 mg Recalled by Granules Pharmaceuticals Inc. Due to...
The Issue: Failed Dissolution Specifications: Out of specification observed during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by Eugia US LLC...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% Moisturizing...
The Issue: LABELING: LABEL MIX-UP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyvinyl Alcohol Ophthalmic Solution 1.4% Recalled by AvKARE Due to...
The Issue: LABELING: LABEL MIX-UP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HemosIL Heparin Calibrators Recalled by Instrumentation Laboratory Due to...
The Issue: Control indicating lower than expected quality control (QC) results and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type). Model/Catalog...
The Issue: Potential for inadvertent retention of biomaterial when the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to 5R 16MM...
The Issue: 5R 16MM knee tibial insert package may contain knee tibial insert 3R 14MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitoring Service Application (MSA). Software to process Recalled by...
The Issue: Not all Electrocardiogram (ECG) events received July 2022-July 2024 were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: glipiZIDE Recalled by Amerisource Health Services LLC Due to Failed...
The Issue: Failed Dissolution Specifications:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FOUZEE SugarLin HERBAL FORMULA capsules Recalled by SHOPPERS- PLAZA Due to...
The Issue: Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective container: Unable to get the solution out of the bottle as the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.