CLASS III Drug recall · Reported 22 Jul 2015 · FDA Enforcement Report

Desmopressin Acetate Tablets recalled by American Health Packaging

American Health Packaging is recalling Desmopressin Acetate Tablets, 0, distributed nationwide in the US. The recall was initiated on 26 Jun 2015 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #:151360, Expiry: 12/31/2016

Quantity recalled341 Cartons

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number: D-1235-2015
FDA event ID: 71634
Recalling firm: American Health Packaging, Columbus, OH
Classification: Class III
Status: Terminated
Recall initiated: 26 Jun 2015
FDA classified: 14 Jul 2015
Reported: 22 Jul 2015
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Packaging Defects

Timeline

26 Jun 2015	Recall initiated by company
14 Jul 2015	Classified by FDA	+18 days
22 Jul 2015	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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.

Where it was distributed

U.S. Nationwide

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

U.S. Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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Other Desmopressin recalls

All 13

Reported	Class	Recall	Company	Reason	Where
22 Apr 2026Drug	CLASS II	Desmopressin Nasal Spray, USP, 10 mcg/ bottle (50 doses) recalled	Apotex	Other	Nationwide
14 Dec 2022Drug	CLASS II	Desmopressin Acetate Tablet, 0.2 mg recalled by RemedyRepack	RemedyRepack	Potency & Assay	MI
7 Dec 2022Drug	CLASS II	Desmopressin Acetate Tablets 0.2mg recalled by Heritage PharmaceuticalsDesmopressin Acetate	Heritage Pharmaceuticals	Potency & Assay	Nationwide
6 Jul 2022Drug	CLASS II	Desmopressin Acetate Tablets, 0.2 mg recalled	Glenmark Pharmaceuticals Inc., USA	Manufacturing (CGMP) Deviations	TX
3 Mar 2021Drug	CLASS II	Desmopressin Acetate Injection USP, 4 mcg/mL Preserved Vial recalled	Teva Pharmaceuticals USA	Sterility	Nationwide