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. 2,400 recalls have been distributed to Nebraska in the last 12 months.
Showing 36881–36900 of 49,150 recalls
Recalled Item: Infant Heel Warmer and Infant Gel Warmer Recalled by CooperSurgical, Inc....
The Issue: Product marketed without a 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicICE v 2.3.14 nordicICE is an image processing software package...
The Issue: The bug causes BOLD activation maps to be visualized as overlays without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zero Xtreme High Performance Fat Burner capsules Recalled by XTREME Z...
The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT) Recalled...
The Issue: Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman Recalled by...
The Issue: Bella Rosa Grated Parmesan Cheese may contain undeclared egg lysozyme.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...
The Issue: Inaccurate scale systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...
The Issue: Customer complaints associated with faulty brake system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silhouette Lift brochure Silhouette Sutures are for use in midface Recalled...
The Issue: Silhouette Lift is recalling the Silhouette Suture brochure because it does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iovera 155 Smart Tip Recalled by Myoscience Inc Due to The expiration date...
The Issue: The expiration date on the outer box label and the pouch label for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Base CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...
The Issue: Crystallization; identified as calcium salt of Ketorolac
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.