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. 2,660 recalls have been distributed to Texas in the last 12 months.
Showing 33161–33180 of 55,713 recalls
Recalled Item: AFC Edamame Soybeans in Pods Recalled by Advanced Fresh Concepts Corp Due to...
The Issue: Product may be contaminated with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg Recalled by Meridian...
The Issue: Defective Delivery System; reports of the device failing to activate which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg Recalled by Meridian...
The Issue: Defective Delivery System; reports of the device failing to activate which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Premark HS Vitamin RDA Premix Recalled by McShare's Inc Due to Product...
The Issue: Product manufactured with an ingredient that contains low levels of soy; soy...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: iXL Advanced Performance Matrix Recalled by McShare's Inc Due to Product...
The Issue: Product manufactured with an ingredient that contains low levels of soy; soy...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Claris Lifesciences Inc...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metronidazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...
The Issue: Product shipped proximate to or past the expiration date listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to Misbranded: Product...
The Issue: Misbranded: Product labeled, Not made with natural rubber latex, may in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...
The Issue: Improperly rated fuses were used in the manufacture of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.