VistaPharm Metoclopramide Oral Solution Recalled: Labeling Error
VistaPharm recalls metoclopramide oral solution due to incorrect labeling. The product may be mispacked with 5mL x 50 instead of 10mL x : 10mL x 50. This is a prescription-only medication.
Lower-risk recall
Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"
Contact the company
What happened, in plain English
VistaPharm is recalling metoclopramide oral solution because the shipping label shows "5 mL x 50" instead of "10 mL x 50." This could lead to incorrect dosing if the product is used as intended. Read more at govinfonow.com/recall/48993-vistapharm-metoclopramide-oral-solution-recalled-labeling-error.
Source Summary by GovInfoNow · govinfonow.com/recall/48993-vistapharm-metoclopramide-oral-solution-recalled-labeling-error · Updated August 19, 2026 · FDA enforcement record: FDA #D-1669-2012
Cite this page
“VistaPharm Metoclopramide Oral Solution Recalled: Labeling Error.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/48993-vistapharm-metoclopramide-oral-solution-recalled-labeling-error. Based on FDA recall #D-1669-2012 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1669-2012%22&limit=1).
Why it’s dangerous
The product label shows the wrong volume (5 mL x 50 instead of 10 mL x 50). This could cause patients to take too little or too much medication if they misinterpret the label.
Who’s affected
Prescription patients who received this metoclopramide oral solution from VistaPharm. Those who use the product as directed are most at risk of incorrect dosing.
How to tell if you have this one
Check for the label that says "5 mL x 50" instead of "10 mL x 50" on the product. This product is prescription-only and manufactured by VistaPharm, Inc. in Largo, FL.
- Brand
VistaPharm- Category
Drug
What to do — step by step
Check Label
Look for the label that says "5 mL x 50" instead of "10 mL x 50" on the product.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- FDA terminated the recall
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1669-2012 (January 19, 2011) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1669-2012 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.