CLASS II Drug recall · Reported 11 Nov 2020 · FDA Enforcement Report

Time-Cap Labs, Inc. Metformin Hydrochloride Extended recalled

Marksans Pharma is recalling Time-Cap Labs, Inc. Metformin Hydrochloride Extended Release Tablets USP 750 mg, distributed nationwide in the US. The recall was initiated on 2 Oct 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesM125E Oct-20; D001F, C084F Nov-20; F073F, E063F Jan-21; F072F Mar-21; J002F, J087F Apr-21; K080F, L056F Jun 21; M046F, Jul-21; 9R9001, Oct-21; 9R9002, Nov-21; 9R0001, 9R0002 Dec-21; 9R0003, XR0016, 9R0004, 9R0005 Mar-22; 9R0006, 9R0007 Apr-22
NDC49483-623, 49483-624
UPC0349483624014, 0349483623109, 0349483623017
Quantity recalled368,976 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-0062-2021
FDA event ID
86530
Recalling firm
Marksans Pharma, Vasco Da Gama, N/A
Manufacturer
TIME CAP LABORATORIES, INC
Classification
Class II
Status
Terminated
Recall initiated
2 Oct 2020
FDA classified
2 Nov 2020
Reported
11 Nov 2020
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Nitrosamine Impurity

Timeline

2 Oct 2020Recall initiated by company
2 Nov 2020Classified by FDA+31 days
11 Nov 2020Published in enforcement report+9 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: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

Nitrosamines are impurities that can form during drug manufacturing or storage. Above the FDA acceptable intake limit, long-term exposure may raise cancer risk. The FDA advises patients to keep taking the medicine until they have a replacement.

Product as listed by the FDA

Time-Cap Labs, Inc. Metformin Hydrochloride Extended Release Tablets USP 750 mg, 100 count bottles, Rx Only Manufactured for: Time-Cap Labs, Inc. 7 Michael Avenue Farmingdale, NY 11735, USA Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83, Verna Indl. Estate. Verna Goa-403 722 India NDC 49483-624-01

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

Which lots are affected?

M125E Oct-20; D001F, C084F Nov-20; F073F, E063F Jan-21; F072F Mar-21; J002F, J087F Apr-21; K080F, L056F Jun 21; M046F, Jul-21; 9R9001, Oct-21; 9R9002, Nov-21; 9R0001, 9R0002 Dec-21; 9R0003, XR0016, 9R0004, 9R0005 Mar-22; 9R0006, 9R0007 Apr-22

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 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.

Other products in this recall event

1 other product · FDA event 86530

This product is part of a recall event; the main page for the event is Time-Cap Labs, Inc. Metformin Hydrochloride recalled by Marksans Pharma.

ReportedClassRecallCompanyReasonWhere
CLASS IITime-Cap Labs, Inc. Metformin Hydrochloride recalled by Marksans PharmaMetformin Hydrochloride Extended ReleaseMarksans PharmaNitrosamine ImpurityNationwide

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