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. 2,581 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,581 in last 12 months

Showing 5528155300 of 55,713 recalls

Medical DeviceFebruary 23, 2012· Tosoh Bioscience Inc

Recalled Item: Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN...

The Issue: Some combinations of Calibrator lots and AlA PACKS resulted in Calibrator #6...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2012· Biomet Spine, LLC

Recalled Item: Timberline Cranial Caudal and Posterior Blades Recalled by Biomet Spine, LLC...

The Issue: Biomet Spine, LLC is recalling the Timberline Cranial Caudal and Posterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2012· American Optisurgical Inc

Recalled Item: TX1 Tissue Removal System Console. Model: TX1 TX1 Tissue Removal Recalled by...

The Issue: Two reasons for recall. 1. Incorrect pressure relief valve installed inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2012· Kerr Corporation

Recalled Item: The brand name of the device is AlgiNot Recalled by Kerr Corporation Due to...

The Issue: The firm recalled the product because it may cure harder than expected...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2012· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Ultra-Short Magnetic Resonance Imaging System Recalled by Toshiba...

The Issue: The firm recalled due to a potentail problem with the position of the hold...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2012· Aesculap Implant Systems

Recalled Item: Columbus Tibia Plateau (component of the Columbus REVISION Knee System)...

The Issue: During an internal quality inspection, the tibia plateau was found to be out...

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...

The Issue: Presence of Foreign Substance(s): There is a potential for foreign...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...

The Issue: Presence of Foreign Substance(s): There is a potential for foreign...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2012· Maquet Cardiovascular Us Sales, Llc

Recalled Item: FLOW-I Anesthesia System The system is intended for use in Recalled by...

The Issue: A technical alarm may be generated on the FLOW-i system when using the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 20, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: enFlow IV Fluid Warmer (510k name: EFLOW IV FLUID WARMER Recalled by Vital...

The Issue: The EnFlow Warmer Strap does not meet the requirements of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module with v2.0 software used Recalled...

The Issue: GE Healthcare became aware of two issues with the Patient Data Module using...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2012· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle Recalled by...

The Issue: A Discrepancy was found on Hitachi AST (HA7 61) package insert. Limitations...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Integra LifeSciences Corp.

Recalled Item: Integra¿ Advansys Medial Lisfranc Plate (MLP) Recalled by Integra...

The Issue: Incorrect technique applied may cause potential rupture of the tibialis...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2012· Afassco Inc

Recalled Item: The finger cots are made out of natural rubber. They Recalled by Afassco Inc...

The Issue: The firm is initiating a field correction because the product(s) were...

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

Class II — Potential Health HazardOngoing
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

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

Class II — Potential Health HazardOngoing
Refund