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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2340123420 of 30,921 recalls

Medical DeviceSeptember 21, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Duracon Flat Tibial Wedge Cemented use only Sterile....

The Issue: Stryker Orthopaedics has received two customer complaints regarding Duracon...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2015· Brainlab AG

Recalled Item: Digital Lightbox Recalled by Brainlab AG Due to Potentially incorrectly...

The Issue: Potentially incorrectly displayed objects when actively deselecting a fused...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2015· Arrow International Inc

Recalled Item: 4FR Single Lumen Pressure Injectable PICC Recalled by Arrow International...

The Issue: Labeling inaccuracy in the Instructions for Use (IFU) and Patient Card. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2015· Philips Electronics North America Corporation

Recalled Item: Philips DuraDiagnost stationary X-ray system Recalled by Philips Electronics...

The Issue: Buttons or keys on the monitor allow the user to turn the volume setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· GE Healthcare

Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...

The Issue: Images may be missing when a system parameter MapRoute is set to a value...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· LifeHealth, LLC

Recalled Item: CC cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...

The Issue: May report values outside the published performance specifications for pH....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· LifeHealth, LLC

Recalled Item: BG cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...

The Issue: May report values outside the published performance specifications for pH....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Medical Device Identification Card for SureScan pacemaker...

The Issue: Some Medical Device Identification Cards provided to SureScan pacemaker...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2015· Elekta, Inc.

Recalled Item: Monaco Radiation Treatment Planning System. Used to make treatment plans...

The Issue: Dose and MU are incorrect when CT images are viewed from the head, and, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Medtronic Navigation, Inc.

Recalled Item: P/N: 9735023 Recalled by Medtronic Navigation, Inc. Due to Specific use...

The Issue: Specific use conditions can increase the possibility of a screwdriver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Smiths Medical ASD, Inc.

Recalled Item: PORT-A-CATH Plastic Hub Needles Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: The label on the lid stock of the individual needle packages for a portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Encore Medical, Lp

Recalled Item: Reverse Shoulder Prosthesis Stem Impaction Fixture The Turon Recalled by...

The Issue: During the assembly, the impaction forces caused the polymer, black acetal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Encore Medical, Lp

Recalled Item: Turon Shoulder Impaction Fixture The Turon and RSP Recalled by Encore...

The Issue: During the Turon assembly, the impaction forces caused the polymer, black...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Valeant Pharmaceuticals North America LLC

Recalled Item: Valeant Pharmaceuticals North America Model No. Spag-2 Small Particle Size...

The Issue: SPAG-2 6000 Lot J3522070 was released to commerce without being tested for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing