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. 1,025 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,025 in last 12 months

Showing 21521–21540 of 49,150 recalls

DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: TRP/ TARGET up & up intensive relief lubricating eye drop Recalled by...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: CVS Health Natural Tears Lubricant Eye Drops Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: iSolutions ActivEyes Nighttime Lubricant Eye Ointment Preservative Free...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: OCuSOFT Eye Wash Sterile Isotonic Buffered Solution Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: CVS Health Lubricating Gel Drops for Anytime Use Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: ActivEyes Altachlore Sodium Chloride Hypertonicity Opthalmic Ointment...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Walgreens Sodium Chloride Ophthalmic Ointment Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Altaire Sterile Eye Wash Recalled by Altaire Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: OCuSOFT retaine NaCl Ophthalmic Ointment Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets (0.8...

The Issue: Failed Impurities/Degradation Specifications: Kaitlib Fe Tablets has an out...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Equate Comfort Gel Lubricant Eye Gel Twin Pack W-M item #: 552374319...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Accutome Rx Accu-WASH Recalled by Altaire Pharmaceuticals, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: OCuSOFT Tetravisc Forte Tetracaine HCl 0.5 % Sterile Anesthetic Recalled by...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: CVS Health Lubricant Eye Drops for Mild to Moderate Dry Eye Recalled by...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: STERILE FLUORO SSP TRAY Kit Code: MNS11605 - Product Usage: Recalled by...

The Issue: Potential for sterile packaging to be compromised

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Teleflex Medical

Recalled Item: Rusch EasyCath Kit Recalled by Teleflex Medical Due to Potential for product...

The Issue: Potential for product not to be sterile.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 Reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Recalled by...

The Issue: Potential for sterile packaging to be compromised

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Centurion Medical Products Corporation

Recalled Item: DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit Recalled by...

The Issue: Potential for sterile packaging to be compromised

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing