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. 2,684 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,684 in last 12 months

Showing 83818400 of 28,334 recalls

Medical DeviceFebruary 25, 2022· Baxter Healthcare Corporation

Recalled Item: MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S Recalled by...

The Issue: Devices distributed lacked regulatory clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· International Science & Technology, LP, DBA Diamatrix Ltd.

Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...

The Issue: Surgical knives may contain incorrect description printed on handles....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· ROi CPS LLC

Recalled Item: Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled...

The Issue: Recalled devices were packaged in convenience kits.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee multi-purpose Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Carefusion 2200 Inc

Recalled Item: (a) CareFusion Snowden-Pencer Plastics Recalled by Carefusion 2200 Inc Due...

The Issue: The finished device package did not contain the IFU.

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

Class II — Potential Health HazardOngoing