Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,045 recalls have been distributed to Nevada in the last 12 months.
Showing 17761–17780 of 50,223 recalls
Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...
The Issue: Subpotent Drug: FDA analysis found product to be subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aquas PowerFlow Tube Set - Product Usage: The device delivers Recalled by...
The Issue: The product design incorporating a motor driven impeller pump powered by one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32 Recalled...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32 Recalled...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK...
The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM HER-2/neu (H2n) assay Recalled by Siemens Healthcare...
The Issue: Siemens confirmed that the Upper Limit of Normal (ULN) as claimed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge -...
The Issue: Low outlier resultsgenerated with Alkaline Phosphatase (ALPI) Flex reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) Recalled by...
The Issue: Opticross 35 Peripheral Imaging Catheter is being recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health"...
The Issue: The third-party brand latex micro surgical gloves packaged within specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imactis Patient Fiducial (Patient ) Recalled by Imactis Due to The firm has...
The Issue: The firm has received reports concerning the patient fiducial disk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.