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Recalls Medicines 2015

Medicines, 2015

Shortlist up to four to read them side by side.

2,020 medicine recalls FDA’s Enforcement Report published in 2015, newest first; 18,075 in all since 2012.

FDA’s medicine recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 6, 2026.

2,020of 2,020 medicine recallsshown with your filters

By the year FDA published them2026704 2025765 2024657 20231,252 20221,349 20211,016 20201,035 20192,152 20181,426 20171,073 20161,25420152,02020141,562 20131,376 2012434

Filters

FDA’s class Class IClass IIClass III

FDA’s own classes: Class I is the most serious. Each recall’s page quotes FDA’s definition.

Status, in FDA’s file OngoingTerminated

Where it went, in FDA’s words FDA says nationwideAlabamaArizonaArkansasCaliforniaFloridaGeorgiaGuamHawaiiIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMichiganMinnesotaMississippiMissouriMontanaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaOhioOklahomaPennsylvaniaPuerto RicoSouth CarolinaSouth DakotaTennesseeTexasUS Virgin IslandsUtahVermontVirginiaWest VirginiaWisconsin

The states FDA’s words on where the product went name. “Nationwide” is its own choice: to FDA it means the fifty states or a significant portion, so a recall is never counted for a state its words don’t name.

The reason Sterility not assuredStrength, purity or how it was madeMay fail, or give wrong resultsPieces of metal, glass or plasticGerms: Listeria, Salmonella, E. coli and othersLabels that are wrong or missingChemicals, metals or drugs that shouldn’t be in it

Grouped from FDA’s own reason for each recall, which every record shows in full.

Published in FDA’s report

Any

In FDA’s record Class IStill ongoing

The list

Filter by product, brand, reason or number

Order the list NewestNewest firstNameName

Medicine recallsPublishedClassStatusWhere

Medicine recall Gabapentin Capsules, USP, 100 mg Failed Capsule/Tablet Specifications: Actavis has received several complaint for clumping and breaking of capsules with some bottles showing popped out bottle… Class IIFDA’s classJan 14, 2015in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedJan 14, 2015ClassClass IIStatusTerminatedWherePuerto Rico
Medicine recall J-TAN D PD Drops (bromphenirame maleate 1 mg and pseudoephedrine hcl 7.5 mg/ teaspoon), 1 fl oz Labeling: Not Elsewhere Classified: Product is labeled “Dye Free” on front panel but contains Red Dye 40. Class IIFDA’s classJan 7, 2015in FDA’s Enforcement Report4 statesnamed in where it went PublishedJan 7, 2015ClassClass IIStatusTerminatedWhereArkansas, Louisiana, Mississippi and Texas
Medicine recall Entertainer’s Secret Throat Relief, 2.0 FL oz Microbial Contamination of Non Sterile Product; microbial assay reported unacceptable high plate counts and positive for E. Class IIFDA’s classJan 7, 2015in FDA’s Enforcement Report2 statesnamed in where it went PublishedJan 7, 2015ClassClass IIStatusTerminatedWhereIndiana and New York
Medicine recall GINSENG KIANPI PIL, 60 capsules, PRODUCT OF KWEILIN DRUG MANUFACTORY Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared dexamethasone and cyproheptadine which are FDA approved drugs… Class IIFDA’s classJan 7, 2015in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 7, 2015ClassClass IIStatusTerminatedWhereNationwide

Before these 2,017 to 2,020 of 2,020

Nothing matches all of these.

Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.

Source:

FDA, Drug recall enforcement reports. Released Nov 3, 2026. Updated weekly.

Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”

Medicines, 2015

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Side by side

The same published facts for each, in the same order, in their sources’ words.

Every line is what FDA’s record says. Recalls aren’t ranked against each other, and a product no recall names isn’t safe by that.

Hearth Record

The honest record on the places and things your family relies on.

Hearth Record is independent. It is not a government agency and is not affiliated with, endorsed by or sponsored by CMS, SAMHSA, HRSA, CPSC, NHTSA, FDA, USDA or any state agency. Each fact links to the agency’s own record.

Every record here is read from the public record and refreshed when its source publishes.

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How to read a record

Four things every record does, shown on an example record made up for this guide.

An example record, made up for this guide

An example nursing home

Made up for this guide: no real place is shown

Not fully inspected in over two years (CMS flag)

11 health citations at the latest inspection cycle

This home 11

State average 14.3

The state average is 14.3.

Source:

CMS, State and US Averages and Health Deficiencies. Released Oct 28, 2026. Updated monthly.

From the homeNone yet. Replies and paid listings aren’t open, and when they open they will sit here, below the record.

1 of 4

Every fact names its source.

Who published it, when, and how often it changes sit beside each fact, with a link to the agency’s own file.

2 of 4

A number never stands alone.

Each figure comes with the baseline its source gives, such as the state average or the middle of its neighbours, and the date it describes.

3 of 4

What needs attention is marked.

One color marks what an agency flagged or found most serious. Nothing is colored to look safe: a public record can’t certify safety.

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The public record comes first.

Anything a provider adds will sit below the record and say who wrote it. Paying never changes a finding, a rating or the order of results.

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