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. 2,551 recalls have been distributed to Nevada in the last 12 months.
Showing 18981–19000 of 28,334 recalls
Recalled Item: NucliSENS magnetic extraction reagents Recalled by BioMerieux SA Due to A...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unna-Z Recalled by Medline Industries Inc Due to Medline Industries, Inc is...
The Issue: Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3 X10 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Twist Drill PRO ¿4.2mm Recalled by Straumann Manufacturing, Inc....
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Drill 1 Recalled by Straumann Manufacturing, Inc. Due to Drills...
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GalaSHAPE 3D Recalled by Tepha Incorporated Due to Endotoxin values from...
The Issue: Endotoxin values from testing of retains slightly exceeded the established...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTX LCV+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova 2000 Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g Recalled by Oculus Innovative...
The Issue: Firm became aware that professional samples of Ceramax are not meeting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTX LCLP+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestilix Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.