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. 2,642 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,642 in last 12 months

Showing 3944139460 of 55,713 recalls

Medical DeviceNovember 24, 2015· Zimmer, Inc.

Recalled Item: Persona EM Distal Rod Recalled by Zimmer, Inc. Due to Complaints that the...

The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2015· Zimmer, Inc.

Recalled Item: Persona EM Proximal Tube Recalled by Zimmer, Inc. Due to Complaints that the...

The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· ZYTO Technologies, Inc.

Recalled Item: The ZYTO Tower is the input device to program the Recalled by ZYTO...

The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· ZYTO Technologies, Inc.

Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...

The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Intuitive Surgical, Inc.

Recalled Item: 30 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...

The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Intuitive Surgical, Inc.

Recalled Item: 0 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...

The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)...

The Issue: Mitek identified that on VAPR Tripolar 90 Degree Suction Electrode the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...

The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...

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

Class II — Potential Health HazardOngoing
FoodNovember 20, 2015· HEB Retail Support Center

Recalled Item: Mi Tienda Tostaditas Botoneras Rojas packaged in bag Recalled by HEB Retail...

The Issue: Possible presence of metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2015· HEB Retail Support Center

Recalled Item: Mi Tienda Masa Preparada By the Pound packaged in bag Recalled by HEB Retail...

The Issue: Possible presence of metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2015· HEB Retail Support Center

Recalled Item: Mi Tienda Tostada Siveria Large Tostada packaged in bag Recalled by HEB...

The Issue: Possible presence of metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2015· Made In Nature, LLC

Recalled Item: Pacific Superfoods Snack Lava Rock Sriracha Kale Chips Recalled by Made In...

The Issue: Made in Nature is recalling Made In Nature Sriracha Chili Kale Chips and...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2015· Made In Nature, LLC

Recalled Item: Made In Nature Sriracha Chili Kale Chips Recalled by Made In Nature, LLC Due...

The Issue: Made in Nature is recalling Made In Nature Sriracha Chili Kale Chips and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2015· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: FMS 3.5mm Ultra-Aggressive Cutter Shaver Blades Recalled by DePuy Mitek,...

The Issue: Product is incorrectly labeled. The blade configuration in the affected lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Bigwall Enterprises

Recalled Item: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...

The Issue: "The public reason for the recall is that the product is being recalled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: FMS neXtra¿ 3.5mm Aggressive Cutter Shaver Blades Recalled by DePuy Mitek,...

The Issue: Product is incorrectly labeled. The blade configuration in the affected lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: FMS neXtra¿ 3.5mm Full Radius Cutter Shaver Blades Recalled by DePuy Mitek,...

The Issue: Product is incorrectly labeled. The blade configuration in the affected lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Steris Corporation

Recalled Item: AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the...

The Issue: The firm discovered that information printed on the quick magnet is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· DePuy Spine, Inc.

Recalled Item: Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical Recalled by...

The Issue: Manufacturing error within the Torque Handle may prohibit some handles from...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Boston Scientific Corp

Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number:...

The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...

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

Class II — Potential Health HazardOngoing