1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses recalled over foreign material
- Recall date
- October 19, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Johnson & Johnson Vision Care, Inc. recalls 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
- Recall number
- Z-1211-2018
- FDA classification
- Class II
- Brand / firm
- Johnson & Johnson Vision Care, Inc.
- Sold / distributed
- Worldwide distribution. US nationwide including Puerto Rico, Korea, Czech Republic, China, Japan, Great Britain, Austria, Malaysia, Hong Kong, Russia, Taiwan, Singapore, India, and Brazil
Why it was recalled
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
Get recall alerts
Free email alert whenever Johnson & Johnson Vision Care, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Johnson & Johnson Vision Care, Inc.