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. 1,172 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,172 in last 12 months

Showing 8261–8280 of 55,713 recalls

Medical DeviceOctober 9, 2023· Philips Ultrasound, Inc.

Recalled Item: Philips Affiniti 70 Recalled by Philips Ultrasound, Inc. Due to Their is the...

The Issue: Their is the potential that diagnostic ultrasound systems operating with...

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

Class II — Potential Health HazardOngoing
FoodOctober 9, 2023· Betty Lou's Inc

Recalled Item: Stabilyze Sugar Stable Dark Chocolate Peanut Butter Recalled by Betty Lou's...

The Issue: Undeclared Sesame

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 9, 2023· Greenhead Lobster Products LLC

Recalled Item: Frozen and fresh RTE Lobster meat (1 lb. packages to Recalled by Greenhead...

The Issue: Lobster meat may 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 DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· LEONI CIA CABLE SYSTEMS

Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...

The Issue: Users of the patient positioning system ORION System can be faced with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· LEONI CIA CABLE SYSTEMS

Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...

The Issue: Users of the patient positioning system ORION System can be faced with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· Intuitive Surgical, Inc.

Recalled Item: Da Vinci Single-Site Wristed Needle Driver Recalled by Intuitive Surgical,...

The Issue: There is the potential for the needle drive to become dislodged and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...

The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Integra LifeSciences Corp.

Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...

The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2023· Encore Medical, LP

Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling

The Issue: Mislabeling

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Encore Medical, LP

Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling

The Issue: Mislabeling

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2023· Dollar Tree Distribution, Inc.

Recalled Item: Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail...

The Issue: CGMP Deviations: OTC products were stored outside of labeled temperature...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2023· CareFusion 303, Inc.

Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...

The Issue: If "Clear All" selected medications is selected on patient profile, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Visgeneer, Inc.

Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...

The Issue: Due to products distributed without premarket clearance or approvals.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Visgeneer, Inc.

Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...

The Issue: Due to products distributed without premarket clearance or approvals.

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

Class II — Potential Health HazardOngoing
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Oxytocin synthetic Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Clinical TREAT Antifungal Powder Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: CGMP deviations: the product was shipped from the Manufacturer to a Medline...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund