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. 1,866 recalls have been distributed to Texas in the last 12 months.
Showing 50901–50920 of 55,713 recalls
Recalled Item: Carestream DRX Evolution System Recalled by Carestream Health Inc. Due to...
The Issue: Due to potential for an x-ray exposure technique change.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic is providing Healthcare Professionals with important safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic INDURA 1P Intrathecal Catheter Recalled by Medtronic...
The Issue: The Sutureless Connector (SC) Intrathecal Catheter connector has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMC Saddle Product Usage: The Ascension CMC is intended to Recalled by...
The Issue: As a result of a quality review, labelling content discrepancies were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. (Pfizer) is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Chloride Preservative Free Sterile injection Recalled by Abrams...
The Issue: Non-Sterility: The firm's contract testing laboratory found sterility failures.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Uncle Eddies Vegan Oatmeal Chocolate Cookies Recalled by International...
The Issue: International Desserts of Glendale, California is recalling Uncle Eddies...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD MAX Instrument Recalled by Becton Dickinson & Co. Due to Electrical power...
The Issue: Electrical power module installed on some in vitro diagnostic instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Vector Distractor Pin Holding Clamp Recalled by Synthes USA HQ, Inc....
The Issue: Synthes is initiating a voluntary Medical Device removal for specified part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 27023WU Balloon Catheter Recalled by Karl Storz Endoscopy America Inc Due to...
The Issue: Karl Storz Endoscopy-America has initiated the recall of the 27023WU Balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Recalled by...
The Issue: The firm is initiating a Field Safety Correction for the labeling of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...
The Issue: When the bed is put into the chair egress position, the magnets on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large Recalled by...
The Issue: Stryker has received reports from customers indicating post-operative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Glidesheath (tm) Recalled by Terumo Medical Corporation Due to...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Articulated Driver A nonpowered hand-held device intended for...
The Issue: When torque is applied to the Articulated Driver at the maximum angle, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.