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. 2,692 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,692 in last 12 months

Showing 2264122660 of 30,921 recalls

Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Radial Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Synthes (USA) Products LLC

Recalled Item: Cervical Spine Locking Plate (CSLP) System Recalled by Synthes (USA)...

The Issue: DePuy Synthes is initiating a Voluntary Medical Device Recall of lot #...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Central Venous Catheter Sets and Trays The subject Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Pressure Monitoring Sets and Trays The subject sets Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Rymed Technologies, LLC

Recalled Item: InVision-Plus and InVision-Plus Junior Needleless IV Connector Recalled by...

The Issue: Potential for the female luer component of the InVision-Plus IV connector to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Salter Labs

Recalled Item: T-piece Nebulizer with in-line connectors Recalled by Salter Labs Due to...

The Issue: Reports that the T-piece does not fit on the nebulizer.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Rymed Technologies, LLC

Recalled Item: InVision-Plus CS Needleless IV Connector Recalled by Rymed Technologies, LLC...

The Issue: Potential for the female luer component of the InVision-Plus IV connector to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2016· Bard Peripheral Vascular Inc

Recalled Item: Bard Distaflo Vascular Bypass Graft Recalled by Bard Peripheral Vascular Inc...

The Issue: Size mislabeling; the graft is labeled as a 6 mm diameter graft when the...

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

Class II — Potential Health HazardOngoing