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Class III: unlikely to cause harmTerminated

Lupin Pharmaceuticals Gatifloxacin Ophthalmic Solution Recall

Gatifloxacin Ophthalmic Solution, 0

Lupin Pharmaceuticals Inc. · Baltimore, MD

Risk level
Class III
Reported by FDA
Nov 3, 2021
Recall ID
D-0091-2022
Check your lot numberHow we source this data

Summary

Lupin Pharmaceuticals recalled Gatifloxacin Ophthalmic Solution starting Oct 20, 2021. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0091-2022 on Nov 3, 2021. Reason: Failed Stability Specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration. Status: Terminated.

Why it was recalled

Failed Stability Specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration.

Product description

Gatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-435-01.

Lot numbers, UPCs & expiration codes

Lot # H002512, exp. date March 2022

Where it was sold

Nationwide in the USA and Puerto Rico

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-0091-2022
Classification
Class III
Status
Terminated
Recall initiated
Oct 20, 2021
FDA report date
Nov 3, 2021
Quantity
16,272 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Lupin Pharmaceuticals Inc.

Original FDA data

Every field from FDA enforcement report D-0091-2022, exactly as published.

Show all FDA fields
City
Baltimore
State
MD
Status
Terminated
Country
United States
Event ID
88885
Address
Harborplace Tower
Address (line 2)
111 S Calvert St Fl 21st
Code information
Lot # H002512, exp. date March 2022
Postal code
21202-6174
Report date
Nov 3, 2021
Product type
Drugs
Recall number
D-0091-2022
Classification
Class III
Recalling firm
Lupin Pharmaceuticals Inc.
Product quantity
16,272 bottles
Termination date
Aug 23, 2022
Reason for recall
Failed Stability Specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Gatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-435-01.
Distribution pattern
Nationwide in the USA and Puerto Rico
Recall initiation date
Oct 20, 2021
Initial firm notification
Letter
Center classification date
Nov 2, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0091-2022, published Nov 3, 2021. View the source record (openFDA) · FDA enforcement reports

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

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