--- title: "VistaPharm LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search VistaPharm LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/vistapharm-llc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Oct 26, 2023 FDA drug enforcement ### [Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.](https://isitonrecall.com/recall/fda-drug-d-0093-2024-mycophenolate-mofetil-for-oral-suspension-usp-200-mg-ml-rx-only-bottle-manufactured-for-vistapharm-i/) Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water. Class III Reported terminated Distribution: Nationwide and Saudi Arabia [Official source for Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: Vis...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0093-2024%22) Oct 18, 2023 FDA drug enforcement ### [Sucralfate Oral Suspension, 1g per 10mL, 16 oz (414 mL) PET bottle (12 bottles per case), Rx Only, Manufactured and Distributed by: VistaPharm, Inc. Largo, FL 33771 USA, NDC 666...](https://isitonrecall.com/recall/fda-drug-d-0047-2024-sucralfate-oral-suspension-1g-per-10ml-16-oz-414-ml-pet-bottle-12-bottles-per-case-rx-only-manufactu/) Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus. Class I Reported terminated Distribution: USA Nationwide [Official source for Sucralfate Oral Suspension, 1g per 10mL, 16 oz (414 mL) PET bottle (12 bottles per case), Rx Only...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0047-2024%22) Oct 17, 2023 FDA drug enforcement ### [Aminocaproic Acid Oral Solution, 0.25 grams/mL, Rx only, packaged in 8 Fl. Oz. (236.5 mL) HDPE bottles, Manufactured for: VistaPharm, Inc., Largo, FL 33771, UAS, NDC 66689-330-08](https://isitonrecall.com/recall/fda-drug-d-0126-2024-aminocaproic-acid-oral-solution-0-25-grams-ml-rx-only-packaged-in-8-fl-oz-236-5-ml-hdpe-bottles-manu/) Failed Excipient Specifications: high content of ethylene glycol (EG) Class III Reported terminated Distribution: Nationwide USA [Official source for Aminocaproic Acid Oral Solution, 0.25 grams/mL, Rx only, packaged in 8 Fl. Oz. (236.5 mL) HDPE bo...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0126-2024%22) Aug 30, 2023 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](https://isitonrecall.com/recall/fda-drug-d-1149-2023-sucralfate-oral-suspension-1g-per-10ml-for-oral-administration-only-414-ml-bottle-rx-only-manufactur/) Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results Class II Reported 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...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1149-2023%22) ## 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. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/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. ## Keep checking [Search VistaPharm LLC](https://isitonrecall.com/check/?q=VistaPharm%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)