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 14681–14700 of 50,223 recalls

Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS RUB IgG (RBG) Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Estradiol II Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Clostridium Difficile Toxin A&B Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: ProxiDiagnost N90 is multi-functional general R/F systems. Recalled by...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Z-Medica, LLC

Recalled Item: QuikClot Combat Gauze-For Temporary External Use To Control Traumatic...

The Issue: Lack of Packaging seal integrity may result in a sterile barrier breach.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Lyme IgG II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS B.R.A.H.M.S. PROCALCITONIN PCT Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· MEDTECH SAS

Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...

The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 22, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...

The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Lyme IgM II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS DEX@ Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Clostridium Difficile GDH Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Mumps IgG (MPG) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS TOXO IgG Avidity (TXGA) Recalled by bioMerieux, Inc. Due to bioMerieux...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Measles IgG (MSG) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Recalled Item: Testosterone Cypionate Testosterone Propionate Recalled by New Vitalis...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund