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Class I: serious health riskOngoing

Global Pharma Healthcare Private Artificial Tears Recall

Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/…

Global Pharma Healthcare Private Limited · Chennai, N/A

Risk level
Class I
Reported by FDA
Jul 19, 2023
Recall ID
D-0919-2023
Check your lot numberHow we source this data

Summary

Global Pharma Healthcare Private recalled Artificial Tears starting Jan 30, 2023. The FDA classified it as Class I (serious health risk) and published enforcement report D-0919-2023 on Jul 19, 2023. Reason: Non-Sterility: FDA analysis found unopened products to have bacterial contamination. Status: Ongoing.

Why it was recalled

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

Product description

Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.

Lot numbers, UPCs & expiration codes

Lot #: PCMI005, Exp. date AUG-2024; PCMJ001, PCMJ002, PCMJ004, PCMJ005, PCMJ006, PCMJ008, PCMJ009, PCMJ010, PCMJ011, PCMJ012, PCMJ013, PCMJ014, PCMJ015, Exp. date MAR-2025

Where it was sold

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

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0919-2023
Classification
Class I
Status
Ongoing
Recall initiated
Jan 30, 2023
FDA report date
Jul 19, 2023
Quantity
400,008 bottles total for all products
Recall type
Voluntary: Firm initiated
Recalling firm
Global Pharma Healthcare Private Limited

Original FDA data

Every field from FDA enforcement report D-0919-2023, exactly as published.

Show all FDA fields
City
Chennai
Status
Ongoing
Country
India
Event ID
91621
Address
A - 9 Sidco Pharmaceutical Complex
Address (line 2)
Thiruporur
Code information
Lot #: PCMI005, Exp. date AUG-2024; PCMJ001, PCMJ002, PCMJ004, PCMJ005, PCMJ006, PCMJ008, PCMJ009, PCMJ010, PCMJ011, PCMJ012, PCMJ013, PCMJ014, PCMJ015, Exp. date MAR-2025
Report date
Jul 19, 2023
Product type
Drugs
Recall number
D-0919-2023
Classification
Class I
Recalling firm
Global Pharma Healthcare Private Limited
Product quantity
400,008 bottles total for all products
Reason for recall
Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.
Distribution pattern
Product was distributed to two distributors who further distributed Nationwide in the USA.
Recall initiation date
Jan 30, 2023
Initial firm notification
E-Mail
Center classification date
Jul 14, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0919-2023, published Jul 19, 2023. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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