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. 2,678 recalls have been distributed to Nevada in the last 12 months.
Showing 10581–10600 of 28,334 recalls
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: 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.
Recalled Item: Sterile Trac System Thinflap 24 MM Burr Hole Plate Recalled by Biomet, Inc....
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: 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: OSS Polyethylene Tibial Bushing 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: RINGLOC BIPOLAR Hip System Bi Polar Locking Ring Recalled by Biomet, Inc....
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 Reverse Shoulder System Recalled by Biomet, Inc. Due to...
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: 4.0/5.0mm 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: RINGLOC ACETABULAR SYSTEM Self-tapping bone screws Recalled by Biomet, Inc....
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: 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: RingLoc+ Quick Connect Drill Bit 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: RapidFire Clip 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: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to System...
The Issue: System does not trigger a cancel command followed by a reload of the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.