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Class I: serious health riskTerminated

Altaire Pharmaceuticals Carboxymethylcellulose Sodium 0 Recall

Carboxymethylcellulose Sodium 0

Altaire Pharmaceuticals, Inc. · Aquebogue, NY

Risk level
Class I
Reported by FDA
Dec 25, 2013
Recall ID
D-375-2014
Check your lot numberHow we source this data

Summary

Altaire Pharmaceuticals recalled Carboxymethylcellulose Sodium 0 starting Sep 6, 2013. The FDA classified it as Class I (serious health risk) and published enforcement report D-375-2014 on Dec 25, 2013. Reason: Non-Sterility: Customer complaints of mold in the product after use and handling due to the fact that the preservative used in the lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution may not be effective through expiry. Status: Terminated.

Why it was recalled

Non-Sterility: Customer complaints of mold in the product after use and handling due to the fact that the preservative used in the lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution may not be effective through expiry.

Product description

Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution, 1 FL OZ (30 mL) bottle, sold under the following labels: (a) CVS pharmacy brand LUBRICANT EYE DROPS FOR MILD TO MODERATE DRY EYE, Distributed by CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 053357 7 and UPC 0 50428 27364 7; (b) equate brand Lubricant Eye Drops, Distributed by Wal-Mart Stores, Inc., Bentonville, AR 72716, UPC 6 81131 03420 3; and (c) up & up brand lubricant eye drops, Dist. by Target Corporation, Minneapolis, MN 55403, UPC 8 58961 79102 0.

Lot numbers, UPCs & expiration codes

Lot #: 11440, Exp 09/13, labeled for CVS; 11441, Exp 09/13, labeled for CVS; 12042, Exp 01/14, labeled for CVS and Wal-Mart ; 12103, Exp 02/15, labeled for Wal-Mart; 12203, Exp 05/15, labeled for CVS and Wal-Mart; 12207, Exp 05/15, labeled for Wal-Mart; 12293, Exp 08/15, labeled for Wal-Mart; 12352, Exp 09/15, labeled for CVS and Target; and 12356, Exp 09/15, labeled for CVS and Target.

Where it was sold

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-375-2014
Classification
Class I
Status
Terminated
Recall initiated
Sep 6, 2013
FDA report date
Dec 25, 2013
Quantity
363,746 bottles.
Recall type
Voluntary: Firm initiated
Recalling firm
Altaire Pharmaceuticals, Inc.

Original FDA data

Every field from FDA enforcement report D-375-2014, exactly as published.

Show all FDA fields
City
Aquebogue
State
NY
Status
Terminated
Country
United States
Event ID
66217
Address
311 West Lane
Address (line 2)
P.O. Box 849
Code information
Lot #: 11440, Exp 09/13, labeled for CVS; 11441, Exp 09/13, labeled for CVS; 12042, Exp 01/14, labeled for CVS and Wal-Mart ; 12103, Exp 02/15, labeled for Wal-Mart; 12203, Exp 05/15, labeled for CVS and Wal-Mart; 12207, Exp 05/15, labeled for Wal-Mart; 12293, Exp 08/15, labeled for Wal-Mart; 12352, Exp 09/15, labeled for CVS and Target; and 12356, Exp 09/15, labeled for CVS and Target.
Postal code
11931-0849
Report date
Dec 25, 2013
Product type
Drugs
Recall number
D-375-2014
Classification
Class I
Recalling firm
Altaire Pharmaceuticals, Inc.
Product quantity
363,746 bottles.
Termination date
Sep 30, 2014
Reason for recall
Non-Sterility: Customer complaints of mold in the product after use and handling due to the fact that the preservative used in the lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution may not be effective through expiry.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution, 1 FL OZ (30 mL) bottle, sold under the following labels: (a) CVS pharmacy brand LUBRICANT EYE DROPS FOR MILD TO MODERATE DRY EYE, Distributed by CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 053357 7 and UPC 0 50428 27364 7; (b) equate brand Lubricant Eye Drops, Distributed by Wal-Mart Stores, Inc., Bentonville, AR 72716, UPC 6 81131 03420 3; and (c) up & up brand lubricant eye drops, Dist. by Target Corporation, Minneapolis, MN 55403, UPC 8 58961 79102 0.
Distribution pattern
Nationwide
Recall initiation date
Sep 6, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Dec 18, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-375-2014, published Dec 25, 2013. 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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