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. 2,708 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,708 in last 12 months

Showing 2198122000 of 55,713 recalls

FoodOctober 7, 2019· CTC Food International Inc

Recalled Item: Orchids Dried Mushroom NET WT. 1 oz. (29G) Product of Recalled by CTC Food...

The Issue: Undeclared sulfites.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 7, 2019· Edwards Lifesciences, LLC

Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...

The Issue: Intermittent communication due to inconsistent crimping of connectors onto...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Nova Ortho-Med Inc

Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...

The Issue: Walkers within the identified serial range have the potential for the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· The Binding Site Group, Ltd.

Recalled Item: Optilite Optilite Rheumatoid Factor Kit Recalled by The Binding Site Group,...

The Issue: Assigned Rheumatoid Factor (RF) calibrator value for calibrator component...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Ventana Medical Systems Inc

Recalled Item: Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System...

The Issue: The firm became aware of a cleaning solution leaking issue from the middle...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Neocis Inc.

Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...

The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Teleflex Medical

Recalled Item: WECK AutoEndo5 Recalled by Teleflex Medical Due to Certain clip appliers...

The Issue: Certain clip appliers have an increase in misloading and/or jamming related...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Teleflex Medical

Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...

The Issue: Certain clip appliers have an increase in misloading and/or jamming related...

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

Class II — Potential Health HazardOngoing