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. 2,708 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,708 in last 12 months

Showing 1990119920 of 30,921 recalls

Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software updates

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Orthosoft, Inc. dba Zimmer CAS

Recalled Item: SmartTools Knee System Orthopedic Stereotaxic Instrument Recalled by...

The Issue: There has been an increase in the number of complaints regarding bent or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Sports Med Repicci II Tibial Components...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2017· Crossroads Extremity Systems Llc

Recalled Item: MotoCLIP(TM) Super Elastic Fusion System Recalled by Crossroads Extremity...

The Issue: Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2017· Merit Medical Systems, Inc.

Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 15, 2017· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit. Dialyzer Recalled by Baxter Healthcare Corporation...

The Issue: Firm has received reports of device operators failing to adhere to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2017· IntroMedic Co., Ltd.

Recalled Item: Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule...

The Issue: When a user switches on MR1100 Receiver, even though the battery was fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2017· Zimmer Biomet, Inc.

Recalled Item: Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital...

The Issue: Digital templates were created with the incorrect files.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2017· Euro Diagnostica AB

Recalled Item: Euro Diagnostica DIASTAT ANA (anti-nuclear antibody) ELISA DIASTAT ANA...

The Issue: Euro Diagnostica has identified a deviation in one of the components of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2017· New Era Orthopaedics, LLc

Recalled Item: Modera Modular Pedicle Screw System Shank Insertion Instrument Recalled by...

The Issue: This is a retrospective recall of an instrument used in spine fusion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2017· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...

The Issue: A damaged temperature sensor at the endoscope's tip can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Remel Inc

Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...

The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...

The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...

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

Class II — Potential Health HazardOngoing