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. 1,648 recalls have been distributed to Vermont in the last 12 months.
Showing 41541–41560 of 47,027 recalls
Recalled Item: Cefepime for Injection USP and Dextrose Injection USP Recalled by B. Braun...
The Issue: Presence of Particulate Matter: The 1g Cefepime for Injection USP and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenytoin Oral Suspension USP 125mg/5mL Recalled by VistaPharm, Inc. Due to...
The Issue: Defective Container: A lidding deformity allowed for the product to have out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...
The Issue: Labeling inconsistency
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...
The Issue: One material batch used for production of the affected parts of the Synthes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Radiometer Medical ApS Recalled by Radiometer America...
The Issue: RADIOMETER become aware that if the ABL90 FLEX is tilted, this may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...
The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...
The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...
The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...
The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM HD ION (various sizes) Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR AUSTIN MOORE FENE. Item codes starting with 45502001 Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.