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. 1,070 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,070 in last 12 months

Showing 13261–13280 of 50,223 recalls

Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: Pain Tray Catalog Number: 9883 Recalled by Busse Hospital Disposables, Inc....

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2022· Preferred Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2022· American Health Packaging

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by American Health Packaging...

The Issue: Impurity failure at 0-time of the repackaged lot.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2022· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Dexamethasone Elixir Recalled by Morton Grove Pharmaceuticals, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: higher than permissible levels...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 21, 2022· SA3, LLC

Recalled Item: Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm Recalled by...

The Issue: Due to failure of microbial testing for total aerobic microbial count (TAMC).

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2022· Baxter Healthcare Corporation

Recalled Item: Liko Universal Twinbar 670 QRH Recalled by Baxter Healthcare Corporation Due...

The Issue: An incorrect center bolt was used in the assembly of the product which could...

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

Class II — Potential Health HazardOngoing
FoodFebruary 20, 2022· Vadilal Industries USA Inc.

Recalled Item: Vadilal Quick Treat Custard Apple Pulp Net Wt Recalled by Vadilal Industries...

The Issue: Product may be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2022· Ansell Healthcare Products LLC

Recalled Item: Gammex Non-Latex PI Green PI-KARE Skin-friendly PI Technology polyisoprene...

The Issue: Transport company failed to stop at the border for required FDA inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· DNA Genotek Inc.

Recalled Item: ORAcollect RNA: ORE-100 Recalled by DNA Genotek Inc. Due to Evaporation of...

The Issue: Evaporation of stabilizing liquid reducing shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· Maquet Medical Systems USA

Recalled Item: Cardiohelp-i Transport Guard with Transport Guard (701072525): is a blood...

The Issue: Potential for a loose cylindrical pin on the Transport Guard that may result...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: 1.5T SIGNA Excite HD Recalled by GE Healthcare, LLC Due to There is...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· NeuMoDx Molecular Inc

Recalled Item: NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems...

The Issue: Potential for false positive results for SARS-CoV-2 in identified lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· DNA Genotek Inc.

Recalled Item: ORAcollect Dx Recalled by DNA Genotek Inc. Due to Evaporation of stabilizing...

The Issue: Evaporation of stabilizing liquid reducing shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· Dollar Tree Distribution, Inc.

Recalled Item: Medical Device products purchased from Family Dollar retail stores located...

The Issue: Potential exposure to rodents and rodent activity in the distribution center.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: 1.5T and 3.0T SIGNA HDx Recalled by GE Healthcare, LLC Due to There is...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: Signa 1.5T TwinSpeed Magnetic Resonance Imaging System Recalled by GE...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: SIGNA Excite 3T. Magnetic Resonance Imaging System Recalled by GE...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2022· Deerfield Imaging, Inc.

Recalled Item: Trumpf Mount Clamp Assembly (table adapter component) Recalled by Deerfield...

The Issue: Reports have been received that after normal or routine lateral forces are...

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

Class II — Potential Health HazardOngoing
FoodFebruary 17, 2022· Abbott Laboratories

Recalled Item: Abbott Similac Sensitive Lactose Sensitivity 22oz. plastic jar. 6 jars...

The Issue: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 17, 2022· FDMR, INC DBA SUJI'S KOREAN CUISINE

Recalled Item: Taiyaki Variety Pack Recalled by FDMR, INC DBA SUJI'S KOREAN CUISINE Due to...

The Issue: Hazelnuts were declared in ingredient statement but not in Contains statement.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund