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. 1,743 recalls have been distributed to Nebraska in the last 12 months.
Showing 41641–41660 of 49,150 recalls
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug.
The Issue: Subpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Injection Recalled by US Compounding Inc Due to Mislabeling
The Issue: Labeling: Label Error on Declared Strength; The outer light protective bags,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser...
The Issue: Laser Aperture label was not applied to certain GYC-1000 Green Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Resuscitator Bag Series: AF1000 Recalled by Ventlab LLC Due to The...
The Issue: The pop-off valve in the defective devices remain open and a squeeze of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part...
The Issue: Alcon CUSTOM-PAK which is supposed to contain a 27G Anterior Chamber Cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...
The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...
The Issue: Surface finish is different than specified. The implant has 30 grit blast on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...
The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...
The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming...
The Issue: All lots of B37 Replacement Screws are being recalled due to potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spicy Yellow Lentil Hummus sold under the Eat Well Embrace Recalled by Hot...
The Issue: Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 5 Layer Fiesta Dip sold under the Trader Joe's brand Recalled by Hot Mama's...
The Issue: Lansal, Inc. (d.b.a. Hot Mama's Foods) is recalling approximately 14,860...
Recommended Action: Do not consume. Return to store for a refund or discard.