Johnson & Johnson Vision Care, Inc.: Medical Device Recall in 2021 - (Recall #: Z-1865-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50

Product Classification:

Class II

Date Initiated: May 6, 2021

Date Posted: June 23, 2021

Recall Number: Z-1865-2021

Event ID: 87947

Reason for Recall:

Potential that a limited number of individual contact lens packages have an incomplete packaging seal.

Status: Terminated

Product Quantity: 6,780 lenses

Code Information:

UPC 733905989612 LOT # BOOWWWL

Distribution Pattern:

Worldwide Distribution. US nationwide, Canada, Germany, Austria, Belgium, France, Luxemburg, Netherland, Portugal, Spain, Sweden, Switzerland, and Trinidad and Tobago.

Voluntary or Mandated:

Voluntary: Firm initiated