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. 933 recalls have been distributed to Nebraska in the last 12 months.
Showing 46361–46380 of 49,150 recalls
Recalled Item: Optetrak Logic Comprehensive Knee Prosthesis System Recalled by Exactech,...
The Issue: A dimensional mismatch was identified which can potentially allow for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Safety Blood Collection Set + Luer Adapter Recalled by Greiner...
The Issue: The VACUETTE Safety Blood Collection Set + Luer Adapter may display leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Hyperbaric Infusion System is a cassette based Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Firebird Spinal Fixation System Recalled by Orthofix, Inc Due to There is a...
The Issue: There is a possibility that the Set Screw (p/n 90-2923) sub-component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Recalled...
The Issue: Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CALCIUM GLUCONATE INJECTION Recalled by Fresenius Kabi USA LLC (FK USA) Due...
The Issue: Labeling: Missing label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vistide (cidofovir) Injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: Particulate matter was found in some vials...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.