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. 1,045 recalls have been distributed to Nebraska in the last 12 months.
Showing 16681–16700 of 49,150 recalls
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment Delivery System with iDMS - Product Usage: used...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...
The Issue: Subpotent Drug: Low out-of-specification assay results for the epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxyzine Hydrochloride Oral Solution Recalled by Morton Grove...
The Issue: Failed Impurities/Degradation Specification: OOS for the following - unknown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vumerity (diroximel fumarate) delayed-release capsule Recalled by Biogen MA...
The Issue: Failed dissolution specifications: out-of-specification test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 400 mg Recalled by Shilpa Medicare Limited Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docetaxel Injection USP 160 mg/8mL (20 mg/mL) Recalled by Shilpa Medicare...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Busulfan Injection 60 mg/10 mL (6 mg/mL) Recalled by Shilpa Medicare Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 100 mg Recalled by Shilpa Medicare Limited Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Roche cobas pro integrated solutions (cobas pro ISE Recalled by Roche...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas 8000 modular analyzer series (i.e. Recalled by Roche Diagnostics...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-110: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-105: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.