FDA Medical Device Recalls (openFDA)
Johnson & Johnson Vision Care, Inc.: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
- Recall number
- Z-1211-2018
- Recalling firm
- Johnson & Johnson Vision Care, Inc.
- Product
- 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
- Status
- Terminated
- Initiated
- 2017-10-19
- Posted
- not on file
- Terminated
- 2020-06-12
- Reason
- Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
- Root cause
- Packaging process control
- Action
- On October 19, 2017, Johnson and Johnson sent letters to their customers stating the recall of ACUVUE and given the instructions to review their inventory, stop using the affected lots, use the enclosed label to return any affected products, contact customer service to arrange the return, even if they do not have any recall product inventory. A contact was provided to each individual letter.
- Quantity
- 56,070
- Distribution
- Worldwide distribution. US nationwide including Puerto Rico, Korea, Czech Republic, China, Japan, Great Britain, Austria, Malaysia, Hong Kong, Russia, Taiwan, Singapore, India, and Brazil
- Lot, serial or model codes
- Lot B00LF41 Exp. 04/2021 Base Curve 8.5 Refractive Power -7.50D -1.25/180 Manufactured at J&J Vision Care Inc. Jacksonville, FL
- 510(k) numbers
- ["K051900"]
- PMA numbers
- not on file
- Product code
- MVN
- Firm FEI
- 1000222023
- Firm city
- Jacksonville
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28