Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,042 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,042 in last 12 months

Showing 36701–36720 of 55,713 recalls

Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

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.

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

Recalled Item: Zenostar MT Color B2 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 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.

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

Recalled Item: Zenostar MT Color D3 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 C2 60ml art. no. 681060. Product Usage: Recalled by...

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
FoodMay 27, 2016· Sid Wainer And Son

Recalled Item: Domaine de Provence La Cucina Tart Shells Produced Exclusively for Recalled...

The Issue: Product contains undeclared allergen, eggs.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 27, 2016· Sid Wainer And Son

Recalled Item: Domaine de Provence Neutral 3"¿ Cone Tart Shells Produced Exclusively...

The Issue: Product contains undeclared allergen, coconut.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 27, 2016· HAITAI CHEONGJU FACTORY

Recalled Item: Matdongsan Peanuts Crunch Snack Recalled by HAITAI CHEONGJU FACTORY Due to...

The Issue: Haitai is recalling Matdongsan Peanut Crunch Snack because it contains...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 27, 2016· Sweet Earth Inc.

Recalled Item: Big Sur Breakfast Burrito Recalled by Sweet Earth Inc. Due to Packaging...

The Issue: Packaging error where a small quantity of Sana Cruz Burritos were packaged...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
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· 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· 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· 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· 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· 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
DrugMay 26, 2016· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM -...

The Issue: Subpotent Drug: Out of Specification assay values on stability for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund