Z-1211-2018 Class II Terminated
FDA device recall Z-1211-2018 was initiated by Johnson & Johnson Vision Care, Inc. on October 19, 2017 and is designated Class II. Reason for recall: Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil. The recall status is terminated (terminated June 12, 2020). Affected quantity: 56,070.
Recall Details
- Product Type
- Devices
- Report Date
- April 4, 2018
- Initiation Date
- October 19, 2017
- Termination Date
- June 12, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 56,070
Product Description
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
Reason for Recall
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Distribution Pattern
Worldwide distribution. US nationwide including Puerto Rico, Korea, Czech Republic, China, Japan, Great Britain, Austria, Malaysia, Hong Kong, Russia, Taiwan, Singapore, India, and Brazil
Code Information
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