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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93322

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
October 26, 2023
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
VistaPharm LLC

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.

D-0093-2024
Recall number
D-0093-2024
Initiated
October 26, 2023
Classification
Class III
Status
Terminated
Recalling firm
VistaPharm LLC
Quantity
11,633 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.

Code information

Lot #: M23400A, M23401A, M23402A, Exp Date. 04/30/2025; M23591A, M23592A, Exp Date. 06/30/2025.

Distribution pattern

Nationwide and Saudi Arabia