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. 2,076 recalls have been distributed to Nevada in the last 12 months.
Showing 3401–3420 of 50,223 recalls
Recalled Item: CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger Recalled...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number:...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A820 myPTM Software Application associated with Medtronic SynchroMed Pump...
The Issue: Product complaints were received describing the A820 myPTM app taking longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Software...
The Issue: Software issues could potentially result in: 1) delays in accessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MSOT Acuity Echo is a Class 4 medical laser Recalled by Ithera Medical...
The Issue: The MSOT Acuity Echo does not include an adequate instruction for safe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a Recalled by...
The Issue: Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK Recalled...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Labeling...
The Issue: Labeling is insufficient regarding delays in access to medication. The firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: babyganics Recalled by Johnson, S C and Son, Inc Due to Failed stability...
The Issue: Failed stability specifications: during routine stability monitoring quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: item 8201919 BAR YST DONUT UNFLD PFD 74x3OZ Recalled by FGF, LLC Due to...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: item 8201846 GEN CHOC HEX DONUT DGH FRZ 144x1.88OZ Recalled by FGF, LLC Due...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: item 8201817 APPLE FILLED PACZKI 66x4 OZ Recalled by FGF, LLC Due to...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: item 8201810 FLUFF BAR 78x2.75 OZ Recalled by FGF, LLC Due to Potential...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: item 8201905 JUST BAKED BLUEBERRY CAKE RING NATURALLY AND ARTIFICIALLY...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: item 8201816 NATURALLY AND ARTIFICIALLY FLAVORED CHEESE PACZKI 66x4OZ...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: item 8201865 JUST BAKED APPLE FRITTERS 72x3OZ Recalled by FGF, LLC Due to...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: item 8201868 GEN TWIST DONUT ZGT PFD 84x1.75 OZ Recalled by FGF, LLC Due to...
The Issue: potential for contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.