CLASS II Drug recall · Reported 2 May 2018 · FDA Enforcement Report

Ibuprofen Tablets USP 800 mg, a) recalled by Time-Cap Laboratories

Time-Cap Laboratories is recalling Ibuprofen Tablets USP 800 mg, a) (, distributed nationwide in the US. The recall was initiated on 11 Jan 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesa) C140C, exp 2/18; b) D049C, D050C, D051C, C142C, C137C, C138C, C141C, exp 2/18; D073C, D074C, exp 3/18
Quantity recalledN/A

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-0693-2018
FDA event ID
79349
Recalling firm
Time-Cap Laboratories, Farmingdale, NY
Classification
Class II
Status
Terminated
Recall initiated
11 Jan 2018
FDA classified
22 Apr 2018
Reported
2 May 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Drug class
Pain Medication

Timeline

11 Jan 2018Recall initiated by company
22 Apr 2018Classified by FDA+101 days
2 May 2018Published in enforcement report+10 days

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

Reason for recall

CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.

Product as listed by the FDA

Ibuprofen Tablets USP 800 mg, a) 100 tablet (NDC 42582-113-10) and b) 500 tablet (NDC 42582-113-18) bottles, Rx, Distributed by; Bi-Coastal Pharma International, Shrewsbury, NJ, Manufactured by: Marksans Pharma, Ltd., Verna, Goa-403 722, India

Where it was distributed

Nationwide.

Nationwide

Questions about this recall

Is Ibuprofen Tablets USP 800 mg, a) ( recalled?

Yes. Time-Cap Laboratories recalled Ibuprofen Tablets USP 800 mg, a) ( on 11 Jan 2018. The recall is Class II and its status is Terminated. Recall number D-0693-2018.

Why was it recalled?

CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.

Which lots are affected?

a) C140C, exp 2/18; b) D049C, D050C, D051C, C142C, C137C, C138C, C141C, exp 2/18; D073C, D074C, exp 3/18

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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