D-0852-2021 Class III Terminated
FDA drug recall D-0852-2021 was initiated by New Vision Pharmaceuticals LLC on September 2, 2021 and is designated Class III. Reason for recall: Subpotent Drug The recall status is terminated (terminated June 21, 2023). Affected quantity: 14,976 FG cartons.
Recall Details
- Product Type
- Drugs
- Report Date
- October 6, 2021
- Initiation Date
- September 2, 2021
- Termination Date
- June 21, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 14,976 FG cartons
Product Description
Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06 FL OZ (120 mL) Total/Nighttime Severe Cold & Flu Relief 8 Pre-Measured Vials 1.01 FL OZ (30 mL) Each 8.12 FL OZ (240 mL) Total Single-Use Vials Mixed Berry Flavor NDC 69842-495-16 UPC 0 50428 64057 9 Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895
Reason for Recall
Subpotent Drug
Distribution Pattern
AL, CA, FL, IN, MI, MO, NJ, NY, PA, RI, SC, TN, TX, VA
Code Information
Lot: 2021-10159 Exp. 06/08/2023