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 2121–2140 of 47,027 recalls
Recalled Item: Servo-u Ventilator System. Model Number: 6688600. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentamicin Injection Recalled by Eugia US LLC Due to Failed Stability...
The Issue: Failed Stability Specifications: Out of specification results for the Color...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Macleods Pharmaceuticals Ltd Due to...
The Issue: Presence of a foreign substance: black hair found embedded in tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spectral CT. Computed tomography X-ray system. Recalled by Philips North...
The Issue: Devices with affected software may experience two unintended motion issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual Product Number: 781173 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Product Number: 781108 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T¿ Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva IT Nova Product Number: 781175 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova Product Number: 781172 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova Product Number: 781106 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Due to identified...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR Product Numbers: (1) 781153 Recalled by Philips North America Due...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Ophthalmic Solution Recalled by Apotex Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOBUTamine Injection Recalled by Pfizer Inc. Due to Discoloration;...
The Issue: Discoloration; discolored solution from cracked vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lacosamide Oral Solution Recalled by Apotex Corp. Due to Defective...
The Issue: Defective Container: This recall is being initiated due to a leaking unit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.