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. 1,132 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,132 in last 12 months

Showing 1521–1540 of 50,223 recalls

Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio. Model Number: 10276755. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
DrugAugust 28, 2025· Ascend Laboratories, LLC

Recalled Item: Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Superpotent...

The Issue: Superpotent drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot. Model Number: 10684333. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Cima.X (DE). Model Number: 11647158. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot Upgrade. Model Number: 10684334. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Connectom.X. Model Number: 11371480. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaCerin Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: 4-N-1 Skin Protectant Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: McKesson Skin Protectant Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Lantiseptic Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Renew Skin Repair Cream Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Hand-E-Foam Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: GelRite Instant Hand Sanitizer Recalled by DermaRite Industries, LLC Due to...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: UltraSure Anti-Perspirant & Deodorant Recalled by DermaRite Industries, LLC...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: San-E-Foam Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaKleen Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund