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. 2,680 recalls have been distributed to Nevada in the last 12 months.
Showing 9981–10000 of 50,223 recalls
Recalled Item: Tempus Pro Patient Monitor is a portable vital signs monitor Recalled by...
The Issue: During internal testing, Regulatory Compliance issues were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl in 0.9% Sodium Chloride Injection Recalled by Nephron...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl in 0.7% Sodium Chloride Injection Recalled by Nephron Sterile...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Evamist (estradiol transdermal spray) Recalled by Padagis US LLC Due to...
The Issue: Failed Content Uniformity Specifications: The Spray Content Uniformity (SCU)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 40 mg (160 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 0.5 mg per 5 mL (100 mcg/mL) Recalled by Denver Solutions,...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes Recalled by...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 20 mg (80 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chukar Cherries Cherry Bombs Bits 'n Pieces Recalled by Chukar Cherry...
The Issue: undeclared hazelnuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.