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. 2,630 recalls have been distributed to Nebraska in the last 12 months.
Showing 5161–5180 of 49,150 recalls
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asli Sesame Seeds Brown 14oz. Recalled by Sands Impex Inc. Dba Asli Fine...
The Issue: Product sample exceeded tolerance for pesticide Fenvalerate
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartMate 3 System Controllers provided within the following HeartMate 3...
The Issue: Left ventricular assist system controller UI membrane/screen may lift along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiple Digital Analog Products labeled as: NobelBiocare...
The Issue: Due to a manufacturing issue, the product has a out of specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch Recalled by...
The Issue: The tube may fall into the surgical site during the grasping process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P Recalled by CareFusion 303, Inc. Due...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FH Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P Recalled by CareFusion 303, Inc. Due...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FH Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK MINI CR-2HH-1FH-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with...
The Issue: Potential for false negative response on the NIM Vital Nerve Monitoring System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FM Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.