Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,508 recalls have been distributed to Alabama in the last 12 months.
Showing 20141–20160 of 28,641 recalls
Recalled Item: Zenostar MT Color Impulse violet 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 D4 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 blue 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 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 grey 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 A3.5 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 B3 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: 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: 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: 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: 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: 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: 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: 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: BrightView XCT Upgrade Model 882454 Recalled by Philips Medical Systems...
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.