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Class II: temporary or reversible health riskCompleted

Altaire Pharmaceuticals Ocusoft Goniosoft Hypromellose 2 Recall

Ocusoft Goniosoft Hypromellose 2

Altaire Pharmaceuticals, Inc. · Aquebogue, NY

Risk level
Class II
Reported by FDA
Nov 27, 2019
Recall ID
D-0397-2020
Check your lot numberHow we source this data

Summary

Altaire Pharmaceuticals recalled Ocusoft Goniosoft Hypromellose 2 starting Jul 2, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0397-2020 on Nov 27, 2019. Reason: Lack of Assurance of Sterility. Status: Completed.

Why it was recalled

Lack of Assurance of Sterility

Product description

Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured for: Ocusoft, Inc., Richmond, TX 77406-0429, NDC 54799-503-15

Lot numbers, UPCs & expiration codes

16260 9/19 17303 10/20 18032 2/21 18235 9/21 18285 11/21 19021 1/22

Where it was sold

U.S.A. Nationwide

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-0397-2020
Classification
Class II
Status
Completed
Recall initiated
Jul 2, 2019
FDA report date
Nov 27, 2019
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Altaire Pharmaceuticals, Inc.

Original FDA data

Every field from FDA enforcement report D-0397-2020, exactly as published.

Show all FDA fields
City
Aquebogue
State
NY
Status
Completed
Country
United States
Event ID
83265
Address
311 W Ln
Address (line 2)
PO Box 849
Code information
16260 9/19 17303 10/20 18032 2/21 18235 9/21 18285 11/21 19021 1/22
Postal code
11931-0849
Report date
Nov 27, 2019
Product type
Drugs
Recall number
D-0397-2020
Classification
Class II
Recalling firm
Altaire Pharmaceuticals, Inc.
Reason for recall
Lack of Assurance of Sterility
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured for: Ocusoft, Inc., Richmond, TX 77406-0429, NDC 54799-503-15
Distribution pattern
U.S.A. Nationwide
Recall initiation date
Jul 2, 2019
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Nov 15, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0397-2020, published Nov 27, 2019. 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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