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. 1,786 recalls have been distributed to Nevada in the last 12 months.
Showing 41201–41220 of 50,223 recalls
Recalled Item: Chicken flavored broth base and seasoning Recalled by Kent Precision Foods...
The Issue: Orrington Farms Chicken Flavored Broth Base & Seasoning, Low Sodium labels...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...
The Issue: Drill set may contain incorrect drill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...
The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...
The Issue: Potential breach of sterile barrier due to defective product tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical CANNULA-CURETTE 12MM Recalled by CooperSurgical, Inc. Due to...
The Issue: The product has been identified to contain an incorrect curette type.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Titan Reverse Shoulder System right and left head cutting templates...
The Issue: A single lot of left and a single lot of right Reverse Shoulder System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Relief ACP Oral Care Gel intended to relieve discomfort from Recalled by...
The Issue: Product sold after April 1, 2014 were inadvertently filled with hydrogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some...
The Issue: Some material of the coating Type CXCPMV3 has potential artifacts showing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meropenem I.V. 1 g is supplied in 30 mL injection vials Recalled by Hospira...
The Issue: Defective Container: Glass vials may crack due to low (thin) out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scrub Care Chlorhexidine Gluconate Solution Recalled by CareFusion 213, LLC...
The Issue: Does Not Meet Monograph: Chlorhexidine Gluconate Surgical Scrub Brush is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nerve Block Tray (Nerve Block convenience kit) Recalled by Centurion Medical...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Pneumo Groups 2-14 Latex Test Recalled by Remel Inc Due to...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTROL P Control for ROTEM delta Thromboelastometry System Recalled by TEM...
The Issue: Some of vials were found to be partially filled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glucose Hexokinase (Liquid) Reagent For the in vitro quantitative...
The Issue: Product is not performing according to specifications. Control 2 does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott m2000sp Recalled by Abbott Molecular Due to Some versions of...
The Issue: Some versions of Application Specifications (App Spec) are incompatible with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Imaging Tray (General Surgery convenience kit) Recalled by...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) Recalled by...
The Issue: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.