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. 2,585 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,585 in last 12 months

Showing 4804148060 of 55,713 recalls

Medical DeviceFebruary 28, 2014· Teleflex Medical

Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...

The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...

The Issue: GE Healthcare has recently become aware of potential safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Bio-Rad Laboratories, Inc.

Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...

The Issue: On a rare occasion the D-10 software might generate an extra result by...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Bard Access Systems

Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...

The Issue: Labeling discrepancy.The label states that the implantable port contains...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Megadyne Medical Products, Inc.

Recalled Item: Hand Control 12FR Suction Coagulator with 10 ft cord and holster Recalled by...

The Issue: Megadyne Medical Products, Inc. is voluntarily recalling Hand Control 12Fr...

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...

The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 26, 2014· Durrset Amigos, Ltd.

Recalled Item: Laura Lynn French Onion Recalled by Durrset Amigos, Ltd. Due to Undeclared Wheat

The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2014· Durrset Amigos, Ltd.

Recalled Item: Roundy's Salsa Con Queso Recalled by Durrset Amigos, Ltd. Due to Undeclared...

The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2014· Durrset Amigos, Ltd.

Recalled Item: HY-TOP FRENCH ONION DIP Recalled by Durrset Amigos, Ltd. Due to Undeclared Wheat

The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2014· Durrset Amigos, Ltd.

Recalled Item: H-E-B Chipotle Con Queso Recalled by Durrset Amigos, Ltd. Due to Undeclared...

The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2014· Durrset Amigos, Ltd.

Recalled Item: HILL COUNTRY FARE Recalled by Durrset Amigos, Ltd. Due to Undeclared Wheat

The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 26, 2014· Wal Mart Stores, Inc

Recalled Item: Safety glasses made with "Rage" frames manufactured between February 20...

The Issue: Fifteen pairs of prescription, safety glasses did not meet required,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2014· Leica Microsystems, Inc.

Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...

The Issue: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2014· Biomet, Inc.

Recalled Item: Part 475630 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...

The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2014· Biomet, Inc.

Recalled Item: Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm Recalled by...

The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw...

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

Class II — Potential Health HazardOngoing