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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2898129000 of 55,713 recalls

Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Thyroid Resilience 120 count bottle packaged in an amber plastic Recalled by...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2018· Get The Tea

Recalled Item: Life Change Fat Burner Recalled by Get The Tea Due to Get The Tea is...

The Issue: Get The Tea is notifying customers that Life Change Fat Burners contain soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2018· Progressive Laboratories, Inc

Recalled Item: Testosterzone 180 count bottle packaged in an amber plastic bottle Recalled...

The Issue: Recalled dietary supplements may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 22, 2018· Ikea North America Srvcs Inc

Recalled Item: Pink flexible Recalled by Ikea North America Srvcs Inc Due to Possible Pest...

The Issue: Possible Pest Contamination at production facility.

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 22, 2018· Roche Diagnostics Corporation

Recalled Item: cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and Recalled...

The Issue: The software responsible for starting scheduled AutoQC measurements...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2018· Roche Diagnostics Corporation

Recalled Item: Cobas b 221<4>Roche OMNI S4 system Recalled by Roche Diagnostics Corporation...

The Issue: The software responsible for starting scheduled AutoQC measurements...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2018· Roche Diagnostics Corporation

Recalled Item: cobas b 221 AutoQC Module Complete Recalled by Roche Diagnostics Corporation...

The Issue: The software responsible for starting scheduled AutoQC measurements...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2018· Roche Diagnostics Corporation

Recalled Item: cobas b 221<6>Roche OMNI S6 system Recalled by Roche Diagnostics Corporation...

The Issue: The software responsible for starting scheduled AutoQC measurements...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2018· Datascope Corporation

Recalled Item: Intra-Aortic Balloon Catheter Mega 8FR 50cc Product Usage: The intra-aortic...

The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2018· CooperVision Inc.

Recalled Item: clariti 1 day (-1.25) 90 pack Recalled by CooperVision Inc. Due to The...

The Issue: The secondary packaging is labeled with an incorrect expiration date.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 21, 2018· CooperVision Inc.

Recalled Item: 56% 1 Day Silicone Hydrogel (-2.50) Recalled by CooperVision Inc. Due to The...

The Issue: The secondary packaging is labeled with an incorrect expiration date.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 21, 2018· Datascope Corporation

Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The...

The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 125II Assay Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: Upon dilution, some patient samples may exhibit over-recovery outside the...

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

Class II — Potential Health HazardOngoing