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 4280142820 of 55,713 recalls

Medical DeviceMarch 30, 2015· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: Potential for clear extension tube to separate from the hub, which could...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2015· Merge Healthcare, Inc.

Recalled Item: Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit) Recalled by Merge Healthcare,...

The Issue: The units may display the alarm "sampling line clogged" after the flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2015· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...

The Issue: A single lot of 18 Gauge, 3.5 inch Tuohy Needles were incorrectly packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2015· OriGen Biomedical, Inc.

Recalled Item: OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE:...

The Issue: Potential for clear extension tube to separate from the hub, which could...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2015· Baylis Medical Corp *

Recalled Item: ProTrack Microcatheter Recalled by Baylis Medical Corp * Due to Baylis...

The Issue: Baylis Medical Company is recalling two lots of ProTrack Microcatheter due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2015· VasoNova, Inc.

Recalled Item: VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number...

The Issue: A limited number of VPS G4 Consoles are being recalled due to noncompliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2015· Becton Dickinson & Co.

Recalled Item: BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) Recalled by Becton...

The Issue: BD has confirmed that one lot of TSA II and Chocolate Agar I-Plates may fail...

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

Class III — Low RiskOngoing
Medical DeviceMarch 27, 2015· Amtryke LLC

Recalled Item: AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle....

The Issue: Product is being recalled due to complaints of cracked frames.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2015· B. Braun Medical, Inc.

Recalled Item: CONTIPLEX Continuous Peripheral Nerve Block Tray Recalled by B. Braun...

The Issue: There is a potential for a hole to be present in the outer tray of a limited...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: the manufacturer, recalled...

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

Class III — Low RiskOngoing
Refund
DrugMarch 26, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Cartia XT (diltiazem HCl extended-release capsules Recalled by Actavis...

The Issue: Presence of Foreign Substance; fine residue or dust identified as aluminum...

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

Class III — Low RiskOngoing
Refund
FoodMarch 26, 2015· Red River Foods Inc

Recalled Item: Style 2 South Africa Macadamia Nuts Recalled by Red River Foods Inc Due to...

The Issue: Baltimore District Office was notified by the Dallas District Office that...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 26, 2015· Mead Johnson Nutrition

Recalled Item: Pregestimil ready to use 20 calorie Recalled by Mead Johnson Nutrition Due...

The Issue: Some Pregestimil 20 Calorie Nursette Bottles from batch EV5A6F were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 26, 2015· Diamedix Corporation

Recalled Item: Diamedix Is-CMV IgG Test Kit Recalled by Diamedix Corporation Due to Product...

The Issue: Product contained an incorrect substrate.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Olympus America Inc.

Recalled Item: EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has...

The Issue: New and validated reprocessing procedures have been issued for the Olympus...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/8 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Round Drain with Trocar Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing