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. 2,279 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,279 in last 12 months

Showing 16811700 of 30,921 recalls

Medical DeviceMay 13, 2025· Cardinal Health 200, LLC

Recalled Item: Kendall SCD Comfort Sleeves Knee Length Small Recalled by Cardinal Health...

The Issue: Incorrect software logic may cause frequent E1 errors (system high...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: MR 5300 Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Elition X Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Ambition S Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: MR 7700 Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Belmont Instrument LLC

Recalled Item: Allon 2001. Part Number: 200-00263 Recalled by Belmont Instrument LLC Due to...

The Issue: An investigation into a report of the patient wrap (ThermoWrap), used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 3.0T Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Upgrade to MR 7700 Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Cardinal Health 200, LLC

Recalled Item: Kendall SCD Blended Comfort Sleeves Knee Length Small - For Recalled by...

The Issue: Incorrect software logic may cause frequent E1 errors (system high...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Evolution Upgrade 3.0T Recalled by Philips North America Llc...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 3.0T CX Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Ambition X Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Elition S Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T CX Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T S Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to Ingenia Elition X Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to dStream for 3.0T Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· Dexcom, Inc.

Recalled Item: Dexcom G7 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...

The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 12, 2025· Fresenius Kabi USA, LLC

Recalled Item: IVENIX INFUSION SYSTEM LVP Blood Products Administration Set Recalled by...

The Issue: Mis-assembly error of Blood Products Administrations Sets where the...

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

Class I — Serious Health HazardOngoing