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. 1,038 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,038 in last 12 months

Showing 38081–38100 of 55,713 recalls

DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Superpotent Drug: one ingredient was found to be above assay specification.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 4 (Papaverine 18 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 0 (PGE 20 mcg/mL) Injection Recalled by Meditech Laboratories, Inc...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 9 (Papaverine 0.9 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Meditech Laboratories, Inc

Recalled Item: Formula 3 (Papaverine 20 mg Recalled by Meditech Laboratories, Inc Due to...

The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2016· Impax Laboratories, Inc.

Recalled Item: Dextroamphetamine Sulfate Tablets USP Recalled by Impax Laboratories, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient Recalled...

The Issue: CGMP Deviations: active pharmaceutical ingredient intermediates failed...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Jubilant Draximage Inc

Recalled Item: SODIUM IODIDE I 131 CAPSULE Recalled by Jubilant Draximage Inc Due to...

The Issue: Labeling: Label Error on Declared Strength

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 11, 2016· Datascope Corporation

Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 5909 14 Pack QPID...

The Issue: There is a potential problem with the cuvette where failure of the cuvette...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 11, 2016· Datascope Corporation

Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET Recalled...

The Issue: There is a potential problem with the cuvette where failure of the cuvette...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 11, 2016· Datascope Corporation

Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 15801 Neonatal...

The Issue: There is a potential problem with the cuvette where failure of the cuvette...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 11, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After importing segmentation results of the left atrium created on the Artis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· RESEARCH INSTRUMENTS LTD - SITE B

Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...

The Issue: The units have been fitted with a potentially faulty power supply cable.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMarch 11, 2016· Awareness Corporation

Recalled Item: Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 Recalled by...

The Issue: Boost Tea is being recalled for potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 11, 2016· Integra York PA, Inc

Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...

The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing