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. 2,722 recalls have been distributed to Nevada in the last 12 months.
Showing 3141–3160 of 50,223 recalls
Recalled Item: Medline procedure kits labeled as: 1) AOP/BASIC EYE PACK-LF Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CSMC/ABDOMINAL HYST PACK-LF Recalled...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) GENERAL ENDOSCOPY PACK Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) A & A KNEE PACK-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ACL ARTHROSCOPY PACK Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CT BIOPSY PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ANGIO PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) L S GYN PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SECTION Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) BREAST PACK-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ANGIO DRAPE PACK (DRLUL)-LF Recalled...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) EYE PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SECTION Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Injection 9% Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility: There is a potential for leakage at the IV...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candida ID Antigen Recalled by Immuno-Mycologics, Inc Due to Candida...
The Issue: Candida Immunodiffusion Antigen may have reduced sensitivity which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origin Data Management software versions 3.1.0 Recalled by Brainlab AG Due...
The Issue: Under certain circumstances, it can occur that patient records from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak with Non-Latex Symbol Recalled by Alcon Research LLC Due to...
The Issue: Customer-designed sterile surgical procedure packs contain latex components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial...
The Issue: Damage to the sterile barrier pouch of catheter, which could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morphine Sulfate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Gel Recalled by Padagis US LLC Due to Defective Container: Some...
The Issue: Defective Container: Some packets may not be fully sealed, potentially...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.