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29 reported ongoing
51 records in this archive. Latest source date Aug 24, 2026.
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.
Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
Class IIReported terminated
Distribution: Nationwide in the US.
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
Class IIReported terminated
Distribution: Nationwide within the United States
Subpotent Drug - Out of specification (OOS) result obtained during monitoring stability study for Assay. Results below specification.
Class IIIReported terminated
Distribution: Distributed in Ohio
Failed Dissolution Specifications: below specification limits for dissolution.
Class IIReported terminated
Distribution: Nationwide in the USA and Puerto Rico
Failed Dissolution Specifications: below specification limits for dissolution.
Class IIReported terminated
Distribution: Nationwide in the USA and Puerto Rico
Superpotent Drug: Out of specification assay result was obtained during stability testing.
Class IIReported terminated
Distribution: Nationwide in the USA
Failed Dissolution Specifications; Low Out of Specification (OOS) results for dissolution.
Class IIReported terminated
Distribution: Nationwide in the U.S.
Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing
Class IIIReported terminated
Distribution: Product was distributed nationwide in the US Market
Failed Dissolution Specifications- Low Out-Of-Specification results obtained during stability testing.
Class IReported terminated
Distribution: Distributed Nationwide in the USA
cGMP Deviations
Class IIReported terminated
Distribution: Nationwide within the United States
Presence of Particulate Matter: Product was found to contain silica and iron oxide
Class IReported terminated
Distribution: Nationwide within the United States
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 51 records, including 29 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
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.
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 and the agency's current notices.
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.