PlainRecalls
FDA Drug Low Class III Terminated

Pilocarpine Hydrochloride Ophthalmic Solution 4% , packaged in 15 mL bottles, Rx Only, Manufactured by Alcon Laboratories, Inc. Fort Worth, Texas 76134 Sandoz Princeton, NJ 08540, NDC 61314-206-15

Reported: May 3, 2017 Initiated: March 22, 2017 #D-0679-2017

Product Description

Pilocarpine Hydrochloride Ophthalmic Solution 4% , packaged in 15 mL bottles, Rx Only, Manufactured by Alcon Laboratories, Inc. Fort Worth, Texas 76134 Sandoz Princeton, NJ 08540, NDC 61314-206-15

Reason for Recall

Failed Impurities/Degradation Specifications.

Details

Units Affected
N/A
Distribution
nationwide
Location
East Hanover, NJ

Frequently Asked Questions

What product was recalled?
Pilocarpine Hydrochloride Ophthalmic Solution 4% , packaged in 15 mL bottles, Rx Only, Manufactured by Alcon Laboratories, Inc. Fort Worth, Texas 76134 Sandoz Princeton, NJ 08540, NDC 61314-206-15. Recalled by Novartis Pharmaceuticals Corp.. Units affected: N/A.
Why was this product recalled?
Failed Impurities/Degradation Specifications.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 3, 2017. Severity: Low. Recall number: D-0679-2017.