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. 2,355 recalls have been distributed to Nebraska in the last 12 months.
Showing 2021–2040 of 28,140 recalls
Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otopore Square outer ear wound dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter TruSystem 7500 Recalled by Baxter Healthcare Corporation Due to There...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopore 8cm nasal/sinus temporary wound dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore Ex Firm 4cm fragmentable nasal dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore Ex Firm 8cm fragmentable nasal dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm fragmentable nasal dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...
The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...
The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.