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. 2,612 recalls have been distributed to Nebraska in the last 12 months.
Showing 7621–7640 of 28,140 recalls
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S with Expandi-Flex/Elbow: a) Recalled by TELEFLEX LLC Due...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR Power Knee OSSUR Power Knee Recalled by Ossur Americas Due to Battery...
The Issue: Battery may dislodge from the Power Knee
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Recalled by Zimmer, Inc. Due to The outer sterile...
The Issue: The outer sterile package cavity has a corner wall thickness that is below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent...
The Issue: Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy Recalled by SenTec AG...
The Issue: Weak skin adhesion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Magnesium (MG) Flex reagent cartridge Siemens Material Number...
The Issue: Dimension Magnesium (MG) Flex reagent cartridge lots may exhibit imprecision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Recalled by...
The Issue: Incorrect information on the Fungitell STAT clamshells containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Core Wire Guide (Safe-T-J Curved) Recalled by Cook Incorporated Due to...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heavy Double Flexible Tipped Wire Guide Recalled by Cook Incorporated Due to...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vinyl Connecting Tube Recalled by Cook Incorporated Due to Cook Medical...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newton Wire Guide (LT Taper/10cm Distal Flexibility) Recalled by Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.