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. 1,812 recalls have been distributed to Nevada in the last 12 months.
Showing 32881–32900 of 50,223 recalls
Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...
The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECULAR MICROSCOPE CEM-530 Recalled by Nidek Inc Due to Software version...
The Issue: Software version 1.08 and 1.09 for the Specular Microscope CEM 530 included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: El Alteno Coconut Shredded Coconut 8 oz. Recalled by El Alteno Due to...
The Issue: Undeclared sulfites
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: El Alteno Raisinettes Dovales 12 oz. Recalled by El Alteno Due to Undeclared...
The Issue: Undeclared milk and soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...
The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...
The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...
The Issue: "We have received reports of patients hair being caught in the e.cam and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...
The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupivacaine Hydrochloride Inj. Recalled by Hospira Inc., A Pfizer Company...
The Issue: Presence of particulate matter: Confirmed customer report for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets Recalled by Amerisource...
The Issue: Failed dissolution specifications - the out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...
The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...
The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets Recalled by Zydus...
The Issue: Failed Dissolution Specifications: Product did not meet dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules Recalled by Golden State...
The Issue: Failed Dissolution Specifications: Out-of-specification results in retained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules Recalled by Golden State...
The Issue: Failed Dissolution Specifications: Out-of-specification results in retained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.