CLASS II Drug recall · Reported 18 Nov 2015 · FDA Enforcement Report

Doxycycline Hyclate Tablets, USP, 100 mg recalled by C. O. Truxton

C. O. Truxton is recalling Doxycycline Hyclate Tablets, USP, 100 mg, distributed nationwide in the US. The recall was initiated on 24 Aug 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 13D0011FP8, Exp 09/15
Quantity recalled287 bottles

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-0164-2016
FDA event ID
72304
Recalling firm
C. O. Truxton, Bellmawr, NJ
Classification
Class II
Status
Terminated
Recall initiated
24 Aug 2015
FDA classified
10 Nov 2015
Reported
18 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Drug class
Antibiotics

Timeline

24 Aug 2015Recall initiated by company
10 Nov 2015Classified by FDA+78 days
18 Nov 2015Published 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

Labeling: Wrong Bar Code

Product as listed by the FDA

Doxycycline Hyclate Tablets, USP, 100 mg, 500-count bottle, Rx only, Distributed by: Truxton Inc. Bellmawr, NJ 08031, Manufactured for: Blu Caribe Dorado, PR 00646 USA, NDC 0463-6000-50 (top panel) NDC 24658-312-05 (side panel)

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Doxycycline Hyclate Tablets, USP, 100 mg recalled?

Yes. C. O. Truxton recalled Doxycycline Hyclate Tablets, USP, 100 mg on 24 Aug 2015. The recall is Class II and its status is Terminated. Recall number D-0164-2016.

Why was it recalled?

Labeling: Wrong Bar Code

Which lots are affected?

Lot # 13D0011FP8, Exp 09/15

Where was it sold?

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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