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. 2,889 recalls have been distributed to Texas in the last 12 months.
Showing 3781–3800 of 30,921 recalls
Recalled Item: ESG-410 Electrosurgical Generator- In conjunction with electrosurgical...
The Issue: Electrosurgical Generators ESG-410 does not power on upon use, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...
The Issue: Specimen collection device may leak after the patient sample swabs have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...
The Issue: Potential for defective test cartridges which may result in false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Call Station Recalled by Securitas Healthcare LLC Due to There is a...
The Issue: There is a risk that alarms will not be received by the Arial Wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Call Station Recalled by Securitas Healthcare LLC Due to This is a...
The Issue: This is a risk that alarms will not be received by the Arial Wireless Nurse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: If blood culture identification panel is used in conjunction with specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: Two (2) reports were sent to customers with an incorrect negative claim on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRANIOTOMY PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A...
The Issue: A non-sterile Mastisol component, which was not labeled as being sterile or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANESTHESIA TURNOVER KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: A non-sterile Mastisol component, which was not labeled as being sterile or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT PEDI CRANI LAMI Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A...
The Issue: A non-sterile Mastisol component, which was not labeled as being sterile or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANESTHESIA TURNOVER KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: A non-sterile Mastisol component, which was not labeled as being sterile or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-VU KUMPE 5F X 40CM -Used for patients in need Recalled by...
The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-VU KUMPE 5F X 65CM -Used for patients in need Recalled by...
The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count Recalled by Embecta Corp. Due...
The Issue: BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Handset with Communicator Recalled by Medtronic Neuromodulation...
The Issue: A subset of the handsets within the kit may not be able to complete the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Afinion 2 Analyzer Recalled by Abbott Diagnostics Technologies AS Due to...
The Issue: Five Afinion 2 (AF2) Analyzer were incorrectly market configured as Moderate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Kit containing the Microtek decanter Recalled by ROi CPS LLC Due to...
The Issue: Decanters may have pin holes and tears in sterile packaging that cannot be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.