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. 1,065 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,065 in last 12 months

Showing 15661–15680 of 50,223 recalls

Medical DeviceMay 14, 2021· Smiths Medical ASD Inc.

Recalled Item: PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit Recalled by Smiths...

The Issue: One lot number of a specific model of ULTRAperc Percutaneous Dilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Recalled...

The Issue: Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2021· Brainlab AG

Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...

The Issue: Display of potential patient movement might be delayed to the user for high...

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

Class II — Potential Health HazardOngoing
DrugMay 14, 2021· Medline Industries Inc

Recalled Item: READYPREP CHG Recalled by Medline Industries Inc Due to Superpotent Drug:...

The Issue: Superpotent Drug: Product is above specification for active ingredient, 2%...

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

Class III — Low RiskOngoing
Refund
DrugMay 14, 2021· Teligent Pharma, Inc.

Recalled Item: Diflorasone Diacetate Ointment USP Recalled by Teligent Pharma, Inc. Due to...

The Issue: Presence of Foreign Substance: Foreign particles observed during routine...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Encore Medical, LP

Recalled Item: DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus Recalled by Encore...

The Issue: Packaging mixup; There is a potential that packaging identified as 12mm knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: InTouch 2131-intended to support a human patient in an acute care setting...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Encore Medical, LP

Recalled Item: DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus Recalled by Encore...

The Issue: Packaging mixup; There is a potential that packaging identified as 12mm knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: IsoGel Air - support surface assists in the prevention and Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Transport Stretcher 747 - a non-powered Recalled by Stryker Medical Division...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: CUB Pediatric Crib- intended to provide a pediatric patient support Recalled...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Stretcher Chair-for use in all acute care hospitals and medical Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: GoBed II MedSurg Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing