Severity
Low
Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.
Reported: November 15, 2023 Initiated: October 26, 2023 #D-0093-2024 11,633 bottles units
VistaPharm LLC issued this FDA Drug recall on November 15, 2023. Classified as Low severity (Class III). Approximately 11,633 bottles units are affected. The recall was issued because: Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.. This recall notice is sourced from official FDA Drug enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
Recall Insight
This FDA Drug action (record #D-0093-2024) was formally reported on November 15, 2023, with the manufacturer initiating the action on October 26, 2023. It is classified under Low severity (Class III), with a current status of Terminated. VistaPharm LLC is listed as the recalling firm, operating out of Largo, FL. Federal records indicate 11,633 bottles units are affected.
The documented reason for this recall is: Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water. Distribution data in the federal record shows the product reached: Nationwide and Saudi Arabia. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 3 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Recall Distribution by Severity Class
Units Affected
11,633 bottles
Related Recalls
6
0 from same agency
Product Description
Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.
Reason for Recall
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
Details
- Recalling Firm
- VistaPharm LLC
- Units Affected
- 11,633 bottles
- Distribution
- Nationwide and Saudi Arabia
- Location
- Largo, FL
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0093-2024 |
| Date reported | November 15, 2023 |
| Date initiated | October 26, 2023 |
| Recalling firm | VistaPharm LLC |
| Units affected | 11,633 bottles |
| Distribution | Nationwide and Saudi Arabia |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
Frequently Asked Questions
What product was recalled? ▼
Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.. Recalled by VistaPharm LLC. Units affected: 11,633 bottles.
Why was this product recalled? ▼
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 15, 2023. Severity: Low. Recall number: D-0093-2024.
Where was the recalled product distributed? ▼
Distribution: Nationwide and Saudi Arabia.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0093-2024) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Data Sources
Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
- Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- U.S. Census Bureau ACS — demographic + housing + income data. census.gov/programs-surveys/acs
- BLS Occupational Employment and Wage Statistics (OEWS) — wage + employment by occupation. bls.gov/oes
- BEA Regional Economic Accounts — GDP + personal income by state/metro. bea.gov/data/regional
- U.S. Census Bureau County Business Patterns — establishment + employment by industry. census.gov/cbp
- IRS Statistics of Income (SOI) — tax-return aggregate data. irs.gov/statistics
- data.gov — U.S. federal open-data portal — discovery layer for additional federal sources. data.gov
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).