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. 2,587 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,587 in last 12 months

Showing 32613280 of 30,921 recalls

Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Custom Inflation Kit Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixSKY Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: MONARCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Blue Diamond Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: StabiliT TOUCH Syringe Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: IntelliSystem Inflation Device Recalled by Merit Medical Systems, Inc. Due...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil ENT Pack that contains the Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Tray that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical T and A Pack that contains Recalled by Windstone Medical...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Septo Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 1.0 and 2.0 Diagnostic Ultrasound Systems Recalled by Siemens...

The Issue: If ultrasound systems with software, are changed from factory default to :...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· B Braun Medical Inc

Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...

The Issue: Incomplete insertion of the patient connector of the Streamline Airless...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· B Braun Medical Inc

Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...

The Issue: Incomplete insertion of the patient connector of the Streamline Airless...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 Recalled by CareFusion 303, Inc. Due to Due...

The Issue: Due to affected devices that may have bent female IUI connector and may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· B Braun Medical Inc

Recalled Item: STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer Recalled...

The Issue: Incomplete insertion of the patient connector of the Streamline Airless...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· B Braun Medical Inc

Recalled Item: STREAMLINE LONG-Tubing to be used to transfer blood between a Recalled by B...

The Issue: Incomplete insertion of the patient connector of the Streamline Airless...

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

Class II — Potential Health HazardOngoing