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. 2,696 recalls have been distributed to Nevada in the last 12 months.
Showing 5281–5300 of 28,334 recalls
Recalled Item: Sterile Water/Saline: Product Name/Product Code: CUP STERILE WATER¿ FOIL LID...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride: Product Name/Product Code: 10ML IV FLUSH STERILE...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon...
The Issue: Certain factory settings for the device were incorrectly described in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE PVP SLN KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVP SOLUTION SING STRL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Mode Stimulator Recalled by Liberty Medical Solutions, LLC Due to The...
The Issue: The instruction manuals that were included with the Multi-Mode Stimulators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- Recalled by Inpeco...
The Issue: Firmware of the Interface Module with Roche Cobas 8000 and Cobas PRO (CO8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE POVIDONE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE STERILE PREP STICK Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion...
The Issue: Ceiling mounted L-arm contains a rotation cover that may potentially be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE BETADINE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura systems with monoplane fixed ceiling mounts: 722001 Allura...
The Issue: Ceiling mounted L-arm contains a rotation cover that may potentially be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE PVP Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sperm separation media are used to separate motile sperm from Recalled by...
The Issue: The lower layer component of a sperm separation Kit does not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Oasis Drain Single W / AC Recalled by Atrium Medical Corporation Due...
The Issue: A sterilization nonconformance prematurely aged the product by 48.3 days,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.