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. 1,023 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,023 in last 12 months

Showing 23901–23920 of 50,223 recalls

DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 15mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 200 mg/Anastrozole 20 mg pellet Recalled by Qualgen, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 87.5mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 25mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 12.5mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 6 mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 10mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 37.5 mg pellet Recalled by Qualgen, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 200mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Canon Medical System, USA, INC.

Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...

The Issue: software malfunction; It was found when a user performs radiography using...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· ASO, LLC

Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...

The Issue: Potential that gauze pads may not be fully sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing