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. 2,369 recalls have been distributed to Vermont in the last 12 months.
Showing 19001–19020 of 27,157 recalls
Recalled Item: Zenostar MT Color C4 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenostar MT Color Impulse orange Recalled by Ivoclar Vivadent, Inc. Due to...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenostar MT Color A1 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenostar MT Color A2 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenostar MT Color B1 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenostar MT Color Impulse brown Recalled by Ivoclar Vivadent, Inc. Due to...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONLINE TDM Vancomycin 100 tests Recalled by Roche Diagnostics Operations,...
The Issue: Roche Diagnostics Operations, Inc. has issued a voluntary recall for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...
The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN...
The Issue: Eight (8) issues were identified which may affect the results generated by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...
The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access software. The firm name on the label is Merge Healthcare...
The Issue: Software displayed incorrect prior reports in the viewport area, only when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to The...
The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Model 882482 Recalled by Philips Medical Systems (Cleveland)...
The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External...
The Issue: LIFEPAK CR Plus Automated External Defibrillators (AED) or LIFEPAK EXPRESS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.