Novartis Pharmaceuticals Corp. recalls Pilocarpine Hydrochloride Ophthalmic Solution 4% , packaged in 15 mL bottles, Rx Only, Manufactured by Alcon Laboratori…
- Recall date
- March 22, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0679-2017
- FDA classification
- Class III
- Brand / firm
- Novartis Pharmaceuticals Corp.
- Sold / distributed
- nationwide
Why it was recalled
Failed Impurities/Degradation Specifications.
Class III means the product violates regulations but is not likely to cause harm.
What 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
Get recall alerts
Free email alert whenever Novartis Pharmaceuticals Corp. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Novartis Pharmaceuticals Corp.