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. 2,659 recalls have been distributed to Nevada in the last 12 months.
Showing 11201–11220 of 28,334 recalls
Recalled Item: Speed Stitch Needle Cassette Recalled by ArthroCare Corporation Due to Due...
The Issue: Due to a supplier error where a portion of the raw material was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 850 Model Number: H3907AD Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Model # H3101RH Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Model # H3100AS Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM670 Pro Model # H3100XB Recalled by GE Healthcare, LLC Due to...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 CZT Model # H3906CW Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM 830 Model # H3910AC Recalled by GE Healthcare, LLC Due to Rotor bearing...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery 670 DR Model # H3100BT Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Recalled by GE Healthcare, LLC Due to Rotor bearing screws were...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...
The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...
The Issue: Masks processed at one site were not maintained at levels of condensation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...
The Issue: Due to non-surgical isolation gowns not meeting all performance test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...
The Issue: The firm registered the product as a Class I device, but has since been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...
The Issue: Connector between support surface and pump may be out of tolerance resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.