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. 2,660 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,660 in last 12 months

Showing 3446134480 of 55,713 recalls

Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Accuray Incorporated

Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...

The Issue: Accuray has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2016· Acumed LLC

Recalled Item: OPT Croutons is a synthetic bone substitute designed for the Recalled by...

The Issue: OPT Croutons, part number 65-0210-S, is recalled due to the result of...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2016· Shire PLC

Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...

The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...

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

Class III — Low RiskOngoing
Refund
FoodDecember 2, 2016· Valley Milk Products

Recalled Item: Sweet Cream Buttermilk Powder in 50 # bags Recalled by Valley Milk Products...

The Issue: Products are recalled due to potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2016· Valley Milk Products

Recalled Item: Non Fat Dry Milk Recalled by Valley Milk Products Due to Potential...

The Issue: Products are recalled due to potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 2, 2016· K2M, Inc

Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...

The Issue: Instruments were developed without adequate consideration given to the need...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Mckesson Medical Imaging

Recalled Item: McKesson Radiology 12.2 - Picture Archive Communication System (PACS)...

The Issue: Issue for customers that use an EMR login or legacy web URL login or legacy...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...

The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Foot Section - BAR5490IVC Recalled by Invacare Corporation Due to A quality...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing