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. 2,722 recalls have been distributed to Nevada in the last 12 months.
Showing 3241–3260 of 50,223 recalls
Recalled Item: Brivo MR355 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Creator Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA MR380 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR360 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by The Harvard Drug...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...
The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...
The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Connected Blood Glucose Meter Recalled by Telcare, LLC Due to...
The Issue: Telcare, LLC has received customer complaints related to battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog...
The Issue: Firm became aware of software issues related to most recent firmware update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.