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. 1,722 recalls have been distributed to Nevada in the last 12 months.
Showing 42621–42640 of 50,223 recalls
Recalled Item: Anspach Pneumatic and Electric Motor Systems. Intended for cutting and...
The Issue: Several attachments and handpieces failed to meet the expected sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROMETHAZINE HYDROCHLORIDE Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Presence of Foreign Tablets: Presence of atenolol 25 mg tablet mixed into...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Devon Supine Recalled by Covidien LLC Due to Straps may separate from the...
The Issue: Straps may separate from the foam pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Rod Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Post Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a potential risk when using LANTIS OIS System client software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...
The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luxurian. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraslim. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Photonica Light Modulator. These include all products labeled as UltraSlim...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging It is a medical image and information Recalled by...
The Issue: The firm has identified a software issue which may cause a discrepancy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The...
The Issue: "Advocate Redi-Code + BMB-BA006A Blood Glucose test strips" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemo-Stat Solution Recalled by Axcentria Pharmaceuticals, LLC Due to...
The Issue: Marketed without an Approved NDA/ANDA; product is being manufactured and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particular Matter: Potential glass delamination and consistent...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particular Matter: Potential glass delamination and consistent...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kenex Radiation Shield and surgical lamps installed with GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage¿ D-Dimer Test PN 98100 Recalled by Alere San Diego, Inc. Due to...
The Issue: Alere initiated this recall because a limited number of Alere Triage¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barricini Milk Chocolate Peanut Butter Pretzels in Net Wt 6.5 oz. plastic...
The Issue: Undeclared wheat. The back panel applied to some containers of milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caravelle CHILI POWDER HOT Net Weight 8 oz. (227G) Recalled by Anhing...
The Issue: Anhing Corporation is recalling Caravelle Brand Chili Powder because it has...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hawaiian Coconut Pudding Recalled by E & M Corporation, Dba Noh Foods...
The Issue: Consumer complaint initiated testing of the product by University of...
Recommended Action: Do not consume. Return to store for a refund or discard.