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. 1,733 recalls have been distributed to Nebraska in the last 12 months.
Showing 45481–45500 of 49,150 recalls
Recalled Item: Streptex* Latex D Recalled by Remel Inc Due to The product may give weak or...
The Issue: The product may give weak or false negative test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobiletta Mira Mobile X-ray System Recalled by Siemens Medical Solutions...
The Issue: Siemens issued a Field Safety Alert about the potential risk to users when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels...
The Issue: The product has the potential for false negative or delayed reaction for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiGiorno pizzeria Recalled by Nestle USA, Inc - Northbrook Pizza Head Office...
The Issue: Plastic contamination. Four pizzas with specific production codes, are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: california Pizza Kitchen crispy thin crust Recalled by Nestle USA, Inc -...
The Issue: Plastic contamination. Four pizzas with specific production codes, are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD SafetyGlide Allergy. Sterile Allergy Treatment Syringe Tray. Recalled by...
The Issue: There has been an increase in complaints regarding the needle/safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...
The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...
The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SexVoltz All Natural Herbal Supplement Recalled by Beamonstar Products Due...
The Issue: Marketed Without an Approved NDA/ANDA; products have been found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit Recalled by...
The Issue: cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Velextra All-Natural Herbal Supplement Recalled by Beamonstar Products Due...
The Issue: Marketed Without an Approved NDA/ANDA; products have been found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...
The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...
The Issue: It is possible for an intermittent error to occur in the gantry sensor of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Breathe Medication Cup. For the delivery of liquid medications Recalled...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....
The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...
The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.