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 39021–39040 of 49,150 recalls
Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ikaria Recalled by INO Therapeutics (dba Ikaria) Due to Potential delivery...
The Issue: Potential delivery failure alarm condition. INOmax DSIR with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUA 540 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 101 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADAPTOR Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5 Recalled by Teleflex...
The Issue: The labelling of units from the affected lot indicates that it contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion set due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KYPHON EXPRESS Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The product, labeled as containing, one bevel-tipped instrument and one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System...
The Issue: In case of a system crash, images may not be written to the hard disk and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Honey & Oat Mixers ready-to-eat dry cereal sold under the Recalled by...
The Issue: Undeclared almonds
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Melatonin Control- Released Tablets Recalled by HVL, LLC Due to Bottles...
The Issue: Bottles contained a vegetarian digestive enzyme dietary supplement instead...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: My Spice Sage CUMIN GROUND under the following labels and Recalled by...
The Issue: Cumin may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.