VistaPharm LLC recall records

0 reported ongoing

4 records in this archive. Latest source date Oct 26, 2023.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

FDA drug enforcement

Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle), Rx Only, Manufactured and Distributed by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-305-16

Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results

Class IIReported terminated

Distribution: Distributed nationwide to 68 consignees in the U.S.

Official source for Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle), Rx Only, Ma...

Reasons in these listed records

  • Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
  • Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus.
  • Failed Excipient Specifications: high content of ethylene glycol (EG)
  • Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results

These examples come from this result page and are not a ranking of every recall reason.

Checking VistaPharm LLC

Is there a recall on vistapharm llc right now?

This archive contains 4 records, including 0 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

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What if the search finds no matching record?

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Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

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