Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,901 recalls have been distributed to Nebraska in the last 12 months.
Showing 20161–20180 of 49,150 recalls
Recalled Item: Estradiol Vaginal Inserts USP Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective Delivery System: complaints for difficulty in pushing the plunger...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cool Mint Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EZ Glide Aortic Cannula Recalled by Edwards Lifesciences, LLC Due to Their...
The Issue: Their is a possibility that the cannula may separate from its connector,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer...
The Issue: The locking pin of the front wheel asse mbly of the Evolution Transfer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to The firm...
The Issue: The firm received complaints that the EMPOWR Acetabular Impactor Balls were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eagle 3000 Sterilizer Recalled by Steris Corporation Due to Potential for...
The Issue: Potential for the incorrect pressure safety valve being included in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAPAN CS ELITE FASTPACK Recalled by Haemonetics Corporation Due to Potential...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS5/5+ Bowl Kit-125 mL Autotransfusion Device - Product Usage: its Recalled...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS Elite Fastpack Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS Elite Processing Set (225 ml) Autotransfusion Device - Product Recalled...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Japan CS Elite FASTPACK DISP. SET - 125ML - Product Recalled by Haemonetics...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.