Unrated Drug recall · FDA · Published June 26, 2015

American Health Packaging Recalls Desmopressin Tablets Due to Labeling Error

American Health Packaging recalls specific lots of Desmopressin Acetate Tablets because some are imprinted with the wrong ID (an 'X'). Check your medication packaging.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-1235-2015Drug American Health Packaging ›

Recall notice

Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.

Take action

Contact the company

Recalling firmAmerican Health Packaging2550 John Glenn Ave, Suite A · Columbus, OH 43217-1188

✎ GovInfoNow plain-language explainer

American Health Packaging is recalling a small number of Desmopressin Acetate Tablets, 0.1 mg, because some tablets were incorrectly imprinted with an 'X' on one side. The recall affects only 341 cartons distributed nationwide. The record does not specify if the medication itself is ineffective or dangerous, only that the identification marking is wrong. Read more at govinfonow.com/recall/44115-american-health-packaging-recalls-desmopressin-acetate-tablets-0-1-mg.

Source Summary by GovInfoNow · govinfonow.com/recall/44115-american-health-packaging-recalls-desmopressin-acetate-tablets-0-1-mg · Updated October 12, 2026 · FDA enforcement record: FDA #D-1235-2015

Cite this page

“American Health Packaging Recalls Desmopressin Tablets Due to Labeling Error.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/44115-american-health-packaging-recalls-desmopressin-acetate-tablets-0-1-mg. Based on FDA recall #D-1235-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1235-2015%22&limit=1).

The FDA announced on June 26, 2015, that American Health Packaging is recalling Desmopressin Acetate Tablets due to incorrect imprinting. Some tablets were imprinted with an X on one side instead of the correct identification.

How to tell if you have it

Brand: American Health Packaging
Product: Desmopressin Acetate Tablets, 0.1 mg
NDC: 68084-606-21
Lot #: 151360
Expiry: 12/31/2016
Quantity: 341 Cartons (3 x 10)

The hazard

The hazard involves tablets and capsules imprinted with the wrong identification. Specifically, some Desmopressin Acetate Tablets were incorrectly imprinted with an X on one side.

Context

GovInfoNow's records show American Health Packaging has 41 other recalls on record since July 23, 2012. Other recent recalls of similar products include American Health Packaging Buprenorphine Tablets Recall (Aug. 19, 2026), American Health Packaging Nitrofurantoin Capsules Recall (May 3, 2022), and American Health Packaging Recalls Cyanocobalamin Injection (April 12, 2022). Other recent recalls of similar products include Unichem Recalls Doxazosin 4mg Tablets (Jan. 21, 2026), American Regent Levocarnitine Injection Recall (April 16, 2026), and SpecGx Oxycodone/Acetaminophen Tablets Recall (Dec. 16, 2025).

How to tell if you have this one

Look for Desmopressin Acetate Tablets, 0.1 mg, Rx Only, packed in 30 tablet cartons (3 x 10). Check the NDC: 68084-606-21, Lot #: 151360, and Expiry: 12/31/2016. Verify if the tablets have an 'X' imprinted on one side.

Brand
American Health Packaging
Category
Drug

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “U.S. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 3.1 years after the firm started it.

Jun 26, 2015Firm started the recall
Jul 14, 2015FDA classified it Class III
Jul 22, 2015Published in FDA’s Enforcement Report
Aug 15, 2018FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/44115-american-health-packaging-recalls-desmopressin-acetate-tablets-0-1-mg">American Health Packaging Recalls Desmopressin Tablets Due to Labeling Error (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-1235-2015 (June 26, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1235-2015 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 12, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.