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. 932 recalls have been distributed to Nevada in the last 12 months.
Showing 42761–42780 of 50,223 recalls
Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: Presence of Foreign Substance; some bottles may contain debris that was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxandrolone Tablets Recalled by Upsher Smith Laboratories, Inc. Due to...
The Issue: Labeling: Missing Label; Three cases of product (total of 36 bottles) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Phenylephrine component is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALOPERIDOL DECANOATE INJECTION Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80%...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength Recalled by...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Muro 128 (sodium chloride) hypertonicity ophthalmic ointment Recalled by...
The Issue: Crystallization: Crystal precipitate formation and an increase in the number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Wockhardt Usa Inc....
The Issue: Failed Dissolution Specifications: Failure of dissolution test observed at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Hypertonicity Ophthalmic Ointment Recalled by Bausch & Lomb,...
The Issue: Crystallization: Crystal precipitate formation and an increase in the number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential for biased results when a Multiple Window (MW) code is associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation Systems (Small Recalled by Synthes, Inc. Due to...
The Issue: Labeling changes have been made related to MR (Magnetic Resonance imaging)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems VitD 100 test Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Bicarbonate Concentrate Recalled by Fresenius Medical Care...
The Issue: Naturalyte Liquid Bicarbonate maybe contaminated
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.