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. 1,136 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,136 in last 12 months

Showing 15641–15660 of 55,713 recalls

Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Estradiol II Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS FSH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS RUB IgG (RBG) Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS SARS-COV-2 IgM Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS B.R.A.H.M.S. PROCALCITONIN PCT Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation/RayPlan versions 4 - 11A Recalled by RAYSEARCH LABORATORIES AB...

The Issue: An issue where the combined density in a dose grid voxel partially covered...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2021· Intuitive Surgical, Inc.

Recalled Item: The da Vinci Xi and X surgical systems (IS4000 and Recalled by Intuitive...

The Issue: Incorrect expiration date on its package labeling (shipper box and inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2021· Datascope Corp.

Recalled Item: Cardiosave Li-Ion Battery Pack Recalled by Datascope Corp. Due to A...

The Issue: A Cardiosave Lithium-Ion Battery Pack used during protocol testing failed to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2021· Olympus Corporation of the Americas

Recalled Item: ASC PneumoLiner device Recalled by Olympus Corporation of the Americas Due...

The Issue: Due to manufacturing error, the Pneumoliner Bag Distal Tab that exits the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2021· Philips Ultrasound Inc

Recalled Item: EPIQ CVxi Diagnostic Ultrasound Systems Recalled by Philips Ultrasound Inc...

The Issue: Ultrasound system software issue can cause an EchoNavigator error...

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

Class II — Potential Health HazardOngoing
DrugSeptember 21, 2021· SigmaPharm Laboratories LLC

Recalled Item: Sodium Phenylbutyrate Powder Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Failed Impurities/Degradation Specifications; Out of Specification impurity...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 20, 2021· Vintage Food Corp.

Recalled Item: Mr. Nut brand Dried Oleaster Net Wt: 10.6 OZ (300g). Recalled by Vintage...

The Issue: Undeclared sulfites

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 20, 2021· Smith & Nephew, Inc.

Recalled Item: 6.5MMX165MM CANNULATED SCREW Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The product label incorrectly indicated that the screws are fully threaded,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2021· Arrow International Inc

Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...

The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2021· Arrow International Inc

Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...

The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2021· Arrow International Inc

Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...

The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: The firm has confirmed the potential for ADVIA Chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2021· Arrow International Inc

Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...

The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...

The Issue: The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2021· Bio-Rad Laboratories, Inc.

Recalled Item: BIO-RAD BioPlex 2200 Syphilis Total & RPR Calibrator Recalled by Bio-Rad...

The Issue: Due to two issues: 1) Customer complaints associated with greater than...

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

Class II — Potential Health HazardOngoing