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. 2,862 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,862 in last 12 months

Showing 74617480 of 55,713 recalls

Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: New warnings are being added to the Instructions for Use for all affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: IFU has been updated to include warnings about the risk of the inlet...

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

Class I — Serious Health HazardOngoing
DrugDecember 26, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Amneal...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 26, 2023· Haleon US Holdings LLC

Recalled Item: Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 26, 2023· Haleon US Holdings LLC

Recalled Item: Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 26, 2023· Amerisource Health Services LLC

Recalled Item: Benzonatate Capsules Recalled by Amerisource Health Services LLC Due to...

The Issue: Superpotent drug: Assay results were slightly above specification at the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 26, 2023· GE Medical Systems, SCS

Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...

The Issue: X-ray exposure termination audible signal on Senographe Pristina with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2023· Ossur H / F

Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...

The Issue: Knee batteries may need replacement with conforming batteries to ensure...

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

Class II — Potential Health HazardOngoing
FoodDecember 22, 2023· World Variety Produce Inc dba Melissa's

Recalled Item: Melissa's Hot Kimchi Pickled Napa Cabbage NET WT. 14 oz Recalled by World...

The Issue: Undeclared allergen; fish.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 22, 2023· Nestle Product Technology Center - Nestle Health Science

Recalled Item: Solgar Recalled by Nestle Product Technology Center - Nestle Health Science...

The Issue: Nestle Health Science has initiated a recall of Solgar Glucosamine...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 22, 2023· Onkos Surgical, Inc.

Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling

The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Onkos Surgical, Inc.

Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling

The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Exactamix Pro 1200 Recalled by Baxter Healthcare Corporation Due to...

The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Exactamix Pro 2400 Recalled by Baxter Healthcare Corporation Due to...

The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...

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

Class I — Serious Health HazardOngoing