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. 1,712 recalls have been distributed to Nevada in the last 12 months.
Showing 49201–49220 of 50,223 recalls
Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is...
The Issue: There is a potential to save reports in RadReport with an Incorrect Final...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...
The Issue: When using the syngo Quality Control package the system may not perform as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...
The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...
The Issue: There was an error on the outer labeling of this device. The inner label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....
The Issue: When using the EasyLink Quality Control Package the system may not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This voluntary medical device correction is related to Alcon products...
The Issue: This medical device correction is related to Alcon products that present a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...
The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Pearl Smoked Oyster Water 12 units per case Recalled by Tri-Union...
The Issue: Chicken of the Sea is recalling Oysters supplied by Chicken of the Sea under...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) Chicken of the Sea Whole Oysters Recalled by Tri-Union Seafoods, L.L.C...
The Issue: Chicken of the Sea is recalling Oysters supplied by Chicken of the Sea under...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) Chicken of the Sea Whole Oysters Pieces 24 units per case Recalled by...
The Issue: Chicken of the Sea is recalling Oysters supplied by Chicken of the Sea under...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bumble Bee Fancy Whole Oysters 12/8 oz can. Recalled by Bumble Bee...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...
The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitre powder. Brand "Selected Product" Recalled by Hocean Inc Due to FDA...
The Issue: FDA analysis of the product found that the product consisted of mainly...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMINOPHYLLINE 20ML Recalled by Franck's Lab Inc., d.b.a. Franck's...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DEXAMETHASONE/BACTERIOSTATIC WATER IONTOPHORESIS 0.5MG/5ML(0.1MG/ML)...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPIVACAINE/HYDROMORPHONE Recalled by Franck's Lab Inc., d.b.a. Franck's...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CEFAZOLIN IN ARTIFICIAL TEARS 50MG/ML OPHTHALMIC 10 ML Recalled by Franck's...
The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.