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. 1,095 recalls have been distributed to Nebraska in the last 12 months.
Showing 8821–8840 of 49,150 recalls
Recalled Item: SurgiMend PRS Meshed Recalled by TEI Biosciences, Inc. Due to Possible out...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile CirClamp with 1.45cm Bell Reprocessed Recalled by MEDLINE...
The Issue: The kits incorrectly contain CirClamp subassembly 345CRSAK which results in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend PRS Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TissueMend Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing cabinet devices plugged into any multi-socket outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-7 Recalled by...
The Issue: There are potential risks of the Hemospray powder adhering to the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-10 Recalled by...
The Issue: There are potential risks of the Hemospray powder adhering to the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pain Reliever Recalled by Aurobindo Pharma USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: firm's investigation due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 20 mg added to 0.9% Sodium Chloride 250mL Bag Recalled by...
The Issue: Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARROW Endurance Extended Dwell Peripheral Catheter System Recalled by ARROW...
The Issue: Potential for catheter separation or leakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...
The Issue: Dilator tips may break in the package and in patients during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Patient Safety V3.9.200 to 3.9.600 Recalled by Baxter Healthcare...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Recalled by Philips North America Llc Due to There is a...
The Issue: There is a software login in issue that may prevent the user from logging in.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voalte Patient Safety Recalled by Baxter Healthcare Corporation Due to...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE NON-STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Affected product lots were mislabeled as "STERILE PVP SLN" when they should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.