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. 1,866 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,866 in last 12 months

Showing 4802148040 of 55,713 recalls

DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not OINTMENT 3X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Quent SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not PORTABLE SIPS 7X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Ex PORTABLE SIPS 5X Recalled by Terra-Medica Inc. Due to Penicillin...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to The...

The Issue: The sterile pouch of the devices from this lot may not be completely sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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· 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· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer Recalled by Roche...

The Issue: electrode used beyond the guaranteed in-use 52 week lifetime,may leak and...

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· 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