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. 2,884 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,884 in last 12 months

Showing 50615080 of 55,713 recalls

Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Arthroscopy Pack Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Open Shoulder Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· BioFire Diagnostics, LLC

Recalled Item: FILMARRAY 2.0 INSTRUMENT Recalled by BioFire Diagnostics, LLC Due to...

The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· B Braun Medical Inc

Recalled Item: Infusomat Space Infusion System/ Large Volume Pump Recalled by B Braun...

The Issue: Extension of previous recall RES 92978. Pumps have the potential for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2024· BioFire Diagnostics, LLC

Recalled Item: FILMARRAY TORCH MODULE BOX Recalled by BioFire Diagnostics, LLC Due to...

The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed impurities/degradation specifications: results for unknown impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed impurities/degradation specifications: results for unknown impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed impurities/degradation specifications: results for unknown impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2024· Cypress Medical Products LLC

Recalled Item: General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety Recalled...

The Issue: The syringes that were inadvertently shipped from the Distribution Center....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system Recalled by...

The Issue: The motorized longitudinal movement of the FlexArm stand may be inconsistent...

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

Class II — Potential Health HazardOngoing
FoodAugust 5, 2024· PBM Nutritionals, LLC

Recalled Item: CVS Health brand and HEB Baby brand Premium Infant Formula Recalled by PBM...

The Issue: Product contains levels of Vitamin D above the maximum level permitted.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2024· Zeco LLC

Recalled Item: Rubbing Alcohol (70% Isopropyl Alcohol) Recalled by Zeco LLC Due to CGMP...

The Issue: CGMP Deviations: sterile water not used for production

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2024· Zeco LLC

Recalled Item: HAND-I-SAN Recalled by Zeco LLC Due to CGMP Deviations: sterile water not...

The Issue: CGMP Deviations: sterile water not used for production

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 5, 2024· QUANTUM SURGICAL SAS

Recalled Item: The EPIONE device v1.0.2 is a user controlled Recalled by QUANTUM SURGICAL...

The Issue: Quantum Surgical has become aware that a component (central axis) inside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· MICROVENTION INC.

Recalled Item: ERIC Retrieval Device ER174030 ER176044 The ERIC Retrieval Recalled by...

The Issue: Due to Retrieval Device product labels stating the incorrect expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: ImpellaCP SmartAssistSetAPAC Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Pump 371 Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 SmartAssist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing