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. 2,654 recalls have been distributed to Nebraska in the last 12 months.
Showing 221–240 of 28,140 recalls
Recalled Item: Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience...
The Issue: A smaller open suction catheter, the 8 Fr Suction Catheter, may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY Recalled...
The Issue: Medline Industries, LP is issuing a recall for specific items and lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE...
The Issue: Medline Industries, LP is issuing a recall for specific items and lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CellMek SPS Sample Preparation System Recalled by Beckman Coulter, Inc. Due...
The Issue: Sample preparation system designed to automate staining, lysing, cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Focalyx Fusion Recalled by Focalyx Technologies, LLC. Due to Software device...
The Issue: Software device that is an accessory for image-guided interventional and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters:...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters:...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX Recalled by Philips North America Due to A...
The Issue: A recent software (SW) patch modifies Mobile Event Notification filter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LSL Healthcare Recalled by LSL Healthcare Inc. Due to BD ChloraPrep Triple...
The Issue: BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT...
The Issue: To remove the software applications from certain CT systems as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wondfo Streptococcal A At-Home Self-Test. At-home test for group A Recalled...
The Issue: Product not cleared by the FDA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm Recalled...
The Issue: Increased reports of stent deployment and expansion issues. The most common...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Bisaf Strep A Self-Test. Test for detection of Recalled by...
The Issue: Product not cleared by the FDA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE Recalled by...
The Issue: A specific lot of screws is incorrectly labeled. Screws are labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification...
The Issue: To remove the software applications from certain CT systems as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.