FDA recall record

Bausch & Lomb Sodium Chloride Hypertonicity Ophthalmic Ointment, 5%, 1/8 oz. (3.5 g) tube recall — FDA D-1411-2014

Crystallization: Crystal precipitate formation and an increase in the number of complaints associated with a gritty, sand-like feeling in the eye.

Class IIclassification
D-1411-2014official record ID
Jul 2, 2014report date

Recall record at a glance

Official recordD-1411-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBausch & Lomb, Inc.
Report dateJul 2, 2014
Recall initiation dateApr 10, 2014
Quantity35,253 tubes
LocationTampa, FL, United States

Official product description

Sodium Chloride Hypertonicity Ophthalmic Ointment, 5%, 1/8 oz. (3.5 g) tube per carton, Distributed by Major Pharmaceuticals, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-5315-38, UPC 3 09045 31538 5.

Why the product was recalled

Crystallization: Crystal precipitate formation and an increase in the number of complaints associated with a gritty, sand-like feeling in the eye.

Distribution information

Nationwide, Puerto Rico, Canada, and Hong Kong.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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