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. 2,593 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,593 in last 12 months

Showing 22612280 of 30,921 recalls

Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: MAJOR VASCULAR PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LACERATION TRAY Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: HIP SCOPE Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: OPEN HEART ADULT - SIDE A Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: C-SECTION PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: GENERAL LAPAROSCOPIC PACK-LF Recalled by American Contract Systems Inc Due...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DIAGNOSTIC NEURO IR TRAY Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: CENTRAL LINE PICC Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LABOR & DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters...

The Issue: Devices may have higher than expected amounts of bacterial endotoxin.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: CV BASIC PUMP PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LABOR & DELIVERY PPS Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DR DIULUS INJECTION PACK Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion System (V6 Platform) Recalled by Baxter...

The Issue: There is the potential for missing motor mounting screws, which may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 5, 2025· Beckman Coulter, Inc.

Recalled Item: Access 2 Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2025· Medtronic Perfusion Systems

Recalled Item: Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA Recalled by...

The Issue: Unexpected loose material in the male luer used in the aortic root cannula...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 5, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...

The Issue: There is the potential for missing motor mounting screws, which may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 5, 2025· Medical Information Technology, Inc.

Recalled Item: MEDITECH Expanse Laboratory (LAB) Recalled by Medical Information...

The Issue: Entering multiple keys that trigger input simultaneously may remove data...

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

Class II — Potential Health HazardOngoing