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. 1,025 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,025 in last 12 months

Showing 22041–22060 of 50,223 recalls

Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Infinium Medical, Inc

Recalled Item: CLEO Patient Monitor /Tranquility VS Patient Monitor Recalled by Infinium...

The Issue: The CLEO & Tranquility VS Patient Monitors 510(k) indications for use in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
FoodMay 31, 2019· Izzio Artisan Bakery, LLC

Recalled Item: Izzio Artisan Bakery 100% Rye Bread Recalled by Izzio Artisan Bakery, LLC...

The Issue: 100% Rye Bread may contain undeclared wheat.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Ritussin DM Children & Adults Recalled by Geritrex, LLC Due to cGMP...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Chiesi USA, Inc.

Recalled Item: Zileuton Extended-Release Tablets Recalled by Chiesi USA, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Out of specification result for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium) Recalled by...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Chiesi USA, Inc.

Recalled Item: ZYFLO CR (zileuton) extended-release tablets Recalled by Chiesi USA, Inc....

The Issue: Failed Dissolution Specifications: Out of specification result for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Geri-Tussin DM Recalled by Geritrex, LLC Due to cGMP Deviations:...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Diocto Liquid Docusate Sodium Stool Softener Recalled by Geritrex,...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate Recalled by Geritrex,...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Diphenhydramine Oral Liquid Alcohol Free Recalled by Geritrex, LLC Due to...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Iron Supplement Elixir Ferrous Sulfate Recalled by Geritrex, LLC...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Ritussin DM Double Strength Recalled by Geritrex, LLC Due to cGMP...

The Issue: cGMP Deviations: Products may have microbial contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 30, 2019· Galemed Corporation

Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold with Gas Supply Recalled by...

The Issue: Reports of pressure relief manifold venting gas below the standard pressure.

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

Class I — Serious Health HazardOngoing