Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,509 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,509 in last 12 months

Showing 2016120180 of 28,654 recalls

Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color B4 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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color D2 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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Siemens Healthcare Diagnostics, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Roche Diagnostics Operations, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Exactech, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Exactech, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Merge Healthcare, Inc.

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.

Class II — Potential Health HazardOngoing