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. 2,654 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,654 in last 12 months

Showing 2874128760 of 30,921 recalls

Medical DeviceApril 3, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2013· Synvasive Technology Inc

Recalled Item: Product is distributed by Zimmer (Warsaw Recalled by Synvasive Technology...

The Issue: Various reciprocating and oscillating saw blades were incorrectly labeled....

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14219-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Fresenius Medical Care Holdings, Inc. dba Renal Solutions

Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...

The Issue: Product is being recalled because the combination of the current 50 mg vial,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...

The Issue: In rare instances, channel shifted results have been generated with cobas¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...

The Issue: The firm is recalling the specific lot due to lower than expected results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2013· Sysmex America, Inc.

Recalled Item: The UF-1000i is a fully automated urine particle analyzer intended Recalled...

The Issue: The current Century Break patch did not contain the same setting for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2013· Cordis Corporation

Recalled Item: Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***. No.***466F220A...

The Issue: Correction to provide clarification and additional labeling to minimize...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· GE Healthcare, LLC

Recalled Item: MSK EXTREME MR SCANNER Recalled by GE Healthcare, LLC Due to Coolant supply...

The Issue: Coolant supply lines may leak liquid onto the floor resulting in a slippery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Elekta, Inc.

Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...

The Issue: The problem is that the "static tolerances" from the calibration files...

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

Class II — Potential Health HazardOngoing