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 2548125500 of 30,921 recalls

Medical DeviceOctober 23, 2014· TEM Systems Inc

Recalled Item: ROTROL P Control for ROTEM delta Thromboelastometry System Recalled by TEM...

The Issue: Some of vials were found to be partially filled.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Centurion Medical Products Corporation

Recalled Item: Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)...

The Issue: According to the recall notice received from Hospira, the recall was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Data Innovations, LLC

Recalled Item: JResultNet drivers using ASTM coding language. Calculator/data processing...

The Issue: Software issue resulting in the results of one patient potentially being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Medtest Holdings, Inc.

Recalled Item: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) Recalled by...

The Issue: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2...

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

Class III — Low RiskOngoing
Medical DeviceOctober 22, 2014· Stryker Neurovascular

Recalled Item: GDC-10 360 10mm x 30cm SR Recalled by Stryker Neurovascular Due to Units of...

The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2014· Stryker Neurovascular

Recalled Item: Target 360 Standard 12mm x 30cm Recalled by Stryker Neurovascular Due to...

The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2014· Invivo Corporation

Recalled Item: Philips Expression MR200 MRI Patient Monitoring System. Recalled by Invivo...

The Issue: The MR 200 devices failed the initial power up test due to capacitor short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2014· Stryker Neurovascular

Recalled Item: GDC-18 360 20mm x 33cm Recalled by Stryker Neurovascular Due to Units of GDC...

The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2014· Stryker Neurovascular

Recalled Item: Gateway OTW 2.75mm x 9mm Recalled by Stryker Neurovascular Due to Units of...

The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2014· Stryker Neurovascular

Recalled Item: GDC-10 360 SOFT 3mm x 6cm SR Recalled by Stryker Neurovascular Due to Units...

The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2014· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Disposable Falope-Ring Band Applicator Kits. and Recalled by...

The Issue: All packages of Falope Ring Band Applicator kits are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2014· Baxter Healthcare Corp.

Recalled Item: HomeChoice/HomeChoice Pro Automated Personal Cycler Recalled by Baxter...

The Issue: The keypad buttons on HomeChoice devices may be activated without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Pleural Drainage System Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: 6F x 60 cm Dual Lumen CT PICC Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Peritoneal Drainage System Recalled by Pfm Medical Inc Due to PFM...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Veta Peritoneal Catheter Kit Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Rapid Centesis Catheter Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT 600 ml Drainage Kit Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing