VistaPharm, Inc. is recalling Metoclopramide Oral Solution, USP 10 mg/10 mL sold in 10 mL cups. The recall is due to defective containers where the lids on the unit dose cups are not fully qualified. This issue affects a specific lot distributed across several U.S. states. Read more at govinfonow.com/recall/44125-vistapharm-inc-recalls-metoclopramide-oral-solution-usp-10-mg-10.
“VistaPharm Recalls Metoclopramide Oral Solution Due to Defective Lids.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/44125-vistapharm-inc-recalls-metoclopramide-oral-solution-usp-10-mg-10. Based on FDA recall #D-1831-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1831-2015%22&limit=1).
The FDA announced on June 26, 2015, that VistaPharm, Inc. voluntarily recalled Metoclopramide Oral Solution due to defective container lids that are not fully qualified. The recall affects 84,100 cups distributed in the U.S., including California, Illinois, Louisiana, Ohio, Pennsylvania, and South Carolina.
How to tell if you have it
Brand: VistaPharm
Product: Metoclopramide Oral Solution, USP 10 mg/10 mL
Form: 10 mL cups, Rx only
NDC: 66689-031-01
Lot #: 387500
Expiry: 01/17
The hazard
The hazard involves defective containers where lids on unit dose cups are not fully qualified. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show VistaPharm, Inc. has 19 other recalls on record since January 19, 2011. Other recent recalls of similar products include VistaPharm Pyridostigmine Bromide Oral Solution (September 30, 2022), VistaPharm Clobazam Oral Suspension (January 7, 2022), and VistaPharm NYSTATIN Oral Suspension (September 25, 2020). Other recent recalls of similar products include ANI Pharmaceuticals Estradiol Gel (May 12, 2026), Golden State Medical Prasugrel HCl 10mg Tablets (August 21, 2026), and Micro Labs Dorzolamide/Timolol Eye Drops (July 22, 2026).
How to tell if you have this one
Look for Metoclopramide Oral Solution, USP 10 mg/10 mL in 10 mL cups manufactured by VistaPharm, Inc. Check if the lot number is 387500 and the expiry date is 01/17. The NDC is 66689-031-01.
Brand
VistaPharm
Category
Drug
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “U.S. Including: CA, IL, LA, OH, PA, and SC.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Illinois, Louisiana, Ohio, Pennsylvania, South Carolina.
Recall timeline
FDA terminated this recall 20 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-1831-2015 (June 26, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1831-2015 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 12, 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.