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. 2,697 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,697 in last 12 months

Showing 2264122660 of 55,713 recalls

Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Aesculap Implant Systems LLC

Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...

The Issue: possibility of the sterility batch being insufficiently sterilized

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clotrimazole and Betamethasone Dipropionate Cream USP Recalled by Glenmark...

The Issue: Temperature Abuse: Complaints received of liquidy texture.

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...

The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 6, 2019· Preventice Services, LLC

Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...

The Issue: The device data being collected and transferred to the monitoring center may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2019· Arrow International Inc

Recalled Item: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by...

The Issue: Products may contain the incorrect banner card within the kit

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2019· Arrow International Inc

Recalled Item: 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard Recalled by Arrow...

The Issue: Products may contain the incorrect banner card within the kit

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2019· Zimmer Biomet, Inc.

Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp Recalled by Zimmer...

The Issue: The potential that the end of the shaft could fail to effectively mate with...

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

Class II — Potential Health HazardOngoing
FoodAugust 6, 2019· Amys Kitchen Inc

Recalled Item: Amy's Bowls - Broccoli & Cheddar Bake Recalled by Amys Kitchen Inc Due to...

The Issue: Consumer complaints of black plastic found in product.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2019· PreGel America, Inc.

Recalled Item: PreGel Lemon 50 4.4 lb (2kg) bag Recalled by PreGel America, Inc. Due to...

The Issue: Undeclared Milk. The firm received a complaint that there was milk in the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 1, 2019· Milkweed & Monarch, LLC

Recalled Item: Honey Lavender Recalled by Milkweed & Monarch, LLC Due to Potential...

The Issue: recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 1, 2019· Milkweed & Monarch, LLC

Recalled Item: Sandia Rose Recalled by Milkweed & Monarch, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 1, 2019· Milkweed & Monarch, LLC

Recalled Item: Ginger Spice Recalled by Milkweed & Monarch, LLC Due to Potential Salmonella...

The Issue: recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2019· Aerolase Corporation

Recalled Item: LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to...

The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2019· GN Otometrics

Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...

The Issue: The electrode lead connector has a protruding conductor beyond insulation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2019· Rocket Medical Plc

Recalled Item: Rocket KCH Fetal Bladder Drainage Catheter Model: R57405 Recalled by Rocket...

The Issue: A complaint was received regarding kinking of the device prior to use. If a...

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

Class II — Potential Health HazardOngoing