Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,103 recalls have been distributed to Virginia in the last 12 months.
Showing 11901–11920 of 53,829 recalls
Recalled Item: ERYTHROMYCIN OPHTHALMIC OINTMENT USP 0.5% Recalled by Akorn, Inc. Due to...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cromolyn Sodium Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olopatadine HCl Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artificial Tears OINTMENT Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artificial Tears Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Akorn, Inc. Due to...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olopatadine HCl Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proparacaine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Ophthalmic Solution 0.5% Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GONAK Hypromellose Ophthalmic Demulcent Solution Recalled by Akorn, Inc. Due...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ofloxacin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tobramycin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Jelly USP Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OneLIF Torque Limiting Adapter Recalled by Novapproach Spine LLC Due to The...
The Issue: The torque limiting adapter may not stay locked inside of the ratcheting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superion¿ Indirect Decompression System (IDS) Model Numbers and Size:...
The Issue: Due to Indirect Decompression System devices exhibiting a potential for weld...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action Industries Inc. Disposable Instrument Pack Recalled by...
The Issue: Scissors contained debris.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BASIN SET Recalled by American Contract Systems, Inc. Due to Basin Set...
The Issue: Basin Set labeling error: components within the kit are for the Single Basin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.