American Health Packaging Desmopressin Acetate Tablets Recall

Why it was recalled

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

Product description

Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217. NDC: 68084-606-21.

Lot numbers, UPCs & expiration codes

Lot #:151360, Expiry: 12/31/2016

Where it was sold

U.S. Nationwide

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-1235-2015
Classification: Class III
Status: Terminated
Recall initiated: Jun 26, 2015
FDA report date: Jul 22, 2015
Quantity: 341 Cartons
Recall type: Voluntary: Firm initiated
Recalling firm: American Health Packaging

Original FDA data

Every field from FDA enforcement report D-1235-2015, exactly as published.

Show all FDA fields

City: Columbus
State: OH
Status: Terminated
Country: United States
Event ID: 71634
Address: 2550 John Glenn Ave
Address (line 2): Suite A
Code information: Lot #:151360, Expiry: 12/31/2016
Postal code: 43217-1188
Report date: Jul 22, 2015
Product type: Drugs
Recall number: D-1235-2015
Classification: Class III
Recalling firm: American Health Packaging
Product quantity: 341 Cartons
Termination date: Aug 15, 2018
Reason for recall: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217. NDC: 68084-606-21.
Distribution pattern: U.S. Nationwide
Recall initiation date: Jun 26, 2015
Initial firm notification: Letter
Center classification date: Jul 14, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1235-2015, published Jul 22, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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