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 15141–15160 of 50,223 recalls

Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Contamac Solutions, Inc.

Recalled Item: Nutrifill Scleral Recalled by Contamac Solutions, Inc. Due to Foreign Object...

The Issue: Contact lens solution may contain foreign material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Bard Peripheral Vascular Inc

Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to Potential for needle...

The Issue: Potential for needle protector to become fully dislodge exposing infusion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative detection and...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Health Mart Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Meijer allergy relief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: GoodSense Aller.Ease Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Health Mart Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Perrigo Fexofenadine Hydrochloride tablets Recalled by Perrigo Company PLC...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets Recalled by...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Kroger Allergy Relief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: TopCare Allergy Relief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: up&up allergy relief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund