ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS
Reported: April 4, 2018 Initiated: October 19, 2017 #Z-1209-2018
Product Description
ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS
Reason for Recall
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Details
- Recalling Firm
- Johnson & Johnson Vision Care, Inc.
- Units Affected
- 125,763
- 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
- Location
- Jacksonville, FL
Frequently Asked Questions
What product was recalled? ▼
ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS. Recalled by Johnson & Johnson Vision Care, Inc.. Units affected: 125,763.
Why was this product recalled? ▼
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 4, 2018. Severity: Moderate. Recall number: Z-1209-2018.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11