D-1669-2012 Class III Terminated
FDA drug recall D-1669-2012 was initiated by VistaPharm, Inc. on Jan 19, 2011 and is designated Class III. Reason for recall: Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50," The recall status is terminated (terminated Aug 30, 2012). Affected quantity: 73,800 cups.
Recall Details
- Product Type
- Drugs
- Report Date
- Sep 5, 2012
- Initiation Date
- Jan 19, 2011
- Termination Date
- Aug 30, 2012
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 73,800 cups
Product Description
METOCLOPRAMIDE ORAL SOLUTION, USP 5 mg/5 mL, This cup delivers 10 mL, Rx Only, Manufactured by VistaPharm, Inc., Largo FL33771
Reason for Recall
Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"
Distribution Pattern
Nationwide
Code Information
195900 exp. 01/12.
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1669-2012
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026