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. 2,631 recalls have been distributed to Nevada in the last 12 months.
Showing 14621–14640 of 28,334 recalls
Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Gen.2 Recalled by Roche Diagnostics Corporation Due to New...
The Issue: New endogenous interference claims have been established for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bilirubin Total Gen.3 Recalled by Roche Diagnostics Corporation Due to New...
The Issue: New endogenous interference claims have been established for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant IgM Gen.2 Recalled by Roche Diagnostics Corporation Due to New...
The Issue: New endogenous interference claims have been established for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are...
The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are...
The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These...
The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These...
The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-HAV IgM test System Recalled by Roche Diagnostics Corporation Due to...
The Issue: Potential for erroneous result messages for the Anti-HAV IgM assay when run...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER Cryptococcal Antigen Recalled by Meridian Bioscience Inc Due to An...
The Issue: An enzyme reagent included in the kit is not maintaining stability through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 400 plus analyzer used in the following assays: Recalled by...
The Issue: COBAS INTEGRA¿ 400 plus and cobas c 111 analyzers Additional Extra Wash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 111 with ISE analyzers analyzer used in the Recalled by Roche...
The Issue: COBAS INTEGRA¿ 400 plus and cobas c 111 analyzers Additional Extra Wash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAVIG Portegra or Portegra2 Overhead Counterpoise System (OCS) used in...
The Issue: If the head mount knob is not properly tightened and the operator directly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-44052-VPS2...
The Issue: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-45052-VPS2...
The Issue: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology...
The Issue: There is a potential that Wedge IDs were not included in the DICOM RT PLAN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GelPOINT Path Transanal Procedural Pack with Epix Electrosurgical L-Hook...
The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.