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. 2,723 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,723 in last 12 months

Showing 2098121000 of 55,713 recalls

FoodDecember 26, 2019· Veggie Noodle Co

Recalled Item: Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Broth (11.5 oz...

The Issue: Potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 11827 The device is Recalled by...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: Prometra II Programmable 20mL Pump. Catalog No. 93827 The device Recalled by...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: Prometra II 40mL Pump. Catalog No. 16827 The device is Recalled by Flowonix...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: US Clinical 20mL Programmable Pump. Catalog No. 01827 The device Recalled by...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 91827 The device is Recalled by...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2019· Flowonix Medical Inc

Recalled Item: Prometra II 20mL Pump. Catalog No. 13827 The device is Recalled by Flowonix...

The Issue: A pump alarm function anomaly in the pump firmware code may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: Wave Prep Tubes (1710-03) and single use cups (17--00-24) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Nikon Metrology

Recalled Item: Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225...

The Issue: The manufacturer identified a risk that their products might fail to comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Zimmer Biomet, Inc.

Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...

The Issue: Potential for the expiration date on the outer label that was applied by...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Philips North America, LLC

Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...

The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...

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

Class II — Potential Health HazardOngoing
FoodDecember 23, 2019· Reichel Foods Inc.

Recalled Item: Pro2Snax To The Max snack tray containing Sliced Apples Recalled by Reichel...

The Issue: Products are being recalled due to Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 23, 2019· Reichel Foods Inc.

Recalled Item: Pro2Snax To The Max snack tray containing Sweet Gala Apples Recalled by...

The Issue: Products are being recalled due to Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund