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Class I: serious health riskOngoing

Kilitch Healthcare India Multi-action Relief Drops Recall

Multi-action Relief Drops (Polyvinyl alcohol 0

Kilitch Healthcare India Limited

Risk level
Class I
Reported by FDA
Feb 14, 2024
Recall ID
D-0308-2024
Check your lot numberHow we source this data

Summary

Kilitch Healthcare India recalled Multi-action Relief Drops starting Nov 13, 2023. The FDA classified it as Class I (serious health risk) and published enforcement report D-0308-2024 on Feb 14, 2024. Reason: Non-Sterility. Status: Ongoing.

Why it was recalled

Non-Sterility

Product description

Multi-action Relief Drops (Polyvinyl alcohol 0.5%, Providone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-2254-3

Lot numbers, UPCs & expiration codes

All lots

Where it was sold

Nationwide within the United States

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-0308-2024
Classification
Class I
Status
Ongoing
Recall initiated
Nov 13, 2023
FDA report date
Feb 14, 2024
Quantity
9,216 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Kilitch Healthcare India Limited

Original FDA data

Every field from FDA enforcement report D-0308-2024, exactly as published.

Show all FDA fields
City
Navi Mumbai
Status
Ongoing
Country
India
Event ID
93357
Address
R - 904 905 T T C Industrial Road
Code information
All lots
Report date
Feb 14, 2024
Product type
Drugs
Recall number
D-0308-2024
Classification
Class I
Recalling firm
Kilitch Healthcare India Limited
Product quantity
9,216 bottles
Reason for recall
Non-Sterility
Voluntary / mandated
Voluntary: Firm initiated
Product description
Multi-action Relief Drops (Polyvinyl alcohol 0.5%, Providone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-2254-3
Distribution pattern
Nationwide within the United States
Recall initiation date
Nov 13, 2023
Initial firm notification
Press Release
Center classification date
Feb 5, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0308-2024, published Feb 14, 2024. 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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