CLASS I ONGOING Drug recall · Reported 19 Jul 2023 · FDA Enforcement Report

Delsam Pharma's Artificial Tears recalled by Global Pharma Healthcare

Global Pharma Healthcare Private is recalling Delsam Pharma's Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10, distributed nationwide in the US. The recall was initiated on 30 Jan 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #: PCMH001, PCMH002, PCMH005, PCMH007, Exp. date NOV-2023
Quantity recalled400,008 bottles total for all products

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-0921-2023
FDA event ID
91621
Recalling firm
Global Pharma Healthcare Private, Chennai, N/A
Classification
Class I
Status
Ongoing
Recall initiated
30 Jan 2023
FDA classified
14 Jul 2023
Reported
19 Jul 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Sterility
Drug class
Eye Drops

Timeline

30 Jan 2023Recall initiated by company
14 Jul 2023Classified by FDA+165 days
19 Jul 2023Published in enforcement report+5 days

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

Reason for recall

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.

Where it was distributed

Product was distributed to two distributors who further distributed Nationwide in the USA.

Nationwide

Questions about this recall

Why was it recalled?

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

Which lots are affected?

Lot #: PCMH001, PCMH002, PCMH005, PCMH007, Exp. date NOV-2023

Where was it sold?

Product was distributed to two distributors who further distributed Nationwide in the USA.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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

3 other products · FDA event 91621

This product is part of a recall event; the main page for the event is Artificial Tears (Carboxymethylcellulose Sodium) Lubricant recalled.

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