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. 1,096 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,096 in last 12 months

Showing 21261–21280 of 55,713 recalls

Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G PFC Injection Needle-.D01 GTIN: 8719214221386 Recalled by Vitreq...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...

The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
DrugDecember 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2019· Akorn Inc

Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...

The Issue: Subpotent Drug: Low Out of specification (OOS) assay results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...

The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Nextremity Solutions

Recalled Item: Stratum Lapidus Plate - Small Rt Recalled by Nextremity Solutions Due to The...

The Issue: The product contains a different plate than indicated by the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· Beckman Coulter Inc.

Recalled Item: Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled by Beckman...

The Issue: Due to customer reports it has been determined that the inoculation system...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System Recalled by TELEFLEX...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· CooperSurgical, Inc.

Recalled Item: ADVANCED ENDOSEE System CANNULA Recalled by CooperSurgical, Inc. Due to...

The Issue: Potential for unsealed pouches in two (2) lots of the Endosee Advance...

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

Class II — Potential Health HazardOngoing