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. 1,944 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,944 in last 12 months

Showing 3832138340 of 55,713 recalls

DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Progressive Gourmet Inc.

Recalled Item: Sausage Recalled by Progressive Gourmet Inc. Due to Potential Listeria...

The Issue: Manufactured in a plant where routine environmental swabs tested positive...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Ingredients Corporation Of America

Recalled Item: BIG BOB GIBSON B-B-Q Seasoning and dry rub Recalled by Ingredients...

The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Ingredients Corporation Of America

Recalled Item: ICA GOURMET SEASONINGS Recalled by Ingredients Corporation Of America Due to...

The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Ingredients Corporation Of America

Recalled Item: C & J BUTCHER SHOP Recalled by Ingredients Corporation Of America Due to...

The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Ingredients Corporation Of America

Recalled Item: KD's GOOD STUFF SEASONING Recalled by Ingredients Corporation Of America Due...

The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Ingredients Corporation Of America

Recalled Item: ICA GOURMET SEASONINGS Recalled by Ingredients Corporation Of America Due to...

The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Ingredients Corporation Of America

Recalled Item: ICA GOURMET SEASONINGS Recalled by Ingredients Corporation Of America Due to...

The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Paraffin Type 3 For in vitro diagnostic use....

The Issue: Multiple complaints were received from customers indicating that they...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 16, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...

The Issue: Siemens found a defective part in their production line which could increase...

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

Class II — Potential Health HazardOngoing