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 2352123540 of 30,921 recalls

Medical DeviceAugust 18, 2015· Brainlab AG

Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...

The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Apatech Limited

Recalled Item: Actifuse ABX/Actifuse MIS System A bone void filler intended only Recalled...

The Issue: Baxter Healthcare is issuing a voluntary recall for all lots of Actifuse ABX...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...

The Issue: patient procedure interruption due to a potential system failure

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....

The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Limacorporate S.p.A

Recalled Item: SMR Shoulder/Spalla Trial Humeral Head diameter .42 mm Recalled by...

The Issue: The dimensions of the mating features of the recalled products are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Toshiba American Medical Systems Inc

Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...

The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Limacorporate S.p.A

Recalled Item: SMR Shoulder/Spalla Trial Heads ECC .4 mm Adaptor Recalled by Limacorporate...

The Issue: The dimensions of the mating features of the recalled products are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2015· Abbott Electrophysiology

Recalled Item: FIRMap 60mm Catheter Recalled by Abbott Electrophysiology Due to The...

The Issue: The expiration date was incorrectly printed on the pouch/box labels of 19...

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

Class III — Low RiskOngoing
Medical DeviceAugust 11, 2015· Zimmer, Inc.

Recalled Item: Zimmer Universal Locking System Recalled by Zimmer, Inc. Due to It was found...

The Issue: It was found through review of open Complaints and stock investigations that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· GE Healthcare

Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: The Centricity...

The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for Endure Luxite Envision Optical System Recalled by Alcon...

The Issue: Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· GE Healthcare

Recalled Item: Centricity Universal Viewer Product Usage: The Centricity Universal Viewer...

The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· Synthes (USA) Products LLC

Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...

The Issue: DLS pin breakage during planned implant removal, after uneventful and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2015· Biomet 3i, LLC

Recalled Item: Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver Recalled by...

The Issue: The RASH3N, a hexed, abutment screw driver tip has been labeled and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2015· Biomet 3i, LLC

Recalled Item: Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips Recalled by...

The Issue: RASQ3N, a square, abutment screw driver tip has been labeled and distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Fenestrated Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing