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. 1,045 recalls have been distributed to Nevada in the last 12 months.
Showing 17001–17020 of 50,223 recalls
Recalled Item: Vis-U-All High Temp 7.5"x13.5" Heat Seal Pouch 200 pouches per box Recalled...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - In vitro diagnostic testing of Recalled by...
The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60" (152 cm) Appx 1.9 ml Recalled by ICU Medical, Inc. Due to Due to the...
The Issue: Due to the incorrect filter assembly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...
The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno Recalled by Siemens Medical...
The Issue: When the user changes frame rates from lower frequency (e.g. 10 f/s) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/H MODULAR STEM Recalled by Biomet, Inc. Due to Specific lots of multiple...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium IFS Recalled by Biomet, Inc. Due to Specific lots of multiple...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Total Shoulder System/Bio-Modular Choice Shoulder System...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHOENIX Recalled by Biomet, Inc. Due to Specific lots of multiple sterile...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Fixed Lateral Recalled by Biomet, Inc. Due to Specific lots of...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5/8.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Cancellous Thread Recalled by Biomet, Inc. Due to Specific lots of...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.