Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12 split lots, repackaged in 30 and 90-packs . Intended for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons
Check against the official notice below — it lists the full affected range.
Johnson & Johnson Vision Care is recalling Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear contact lenses with an 8.5 base curve and -3.25 power in specific lot numbers. The company received reports of partially formed contact lenses that appear visibly smaller in diameter, are thicker and stiffer to the touch, and are more darkly tinted blue than normal lenses. The affected product was distributed worldwide, including throughout the United States, Puerto Rico, Canada, Barbados, Japan, and Korea, with a total quantity of 195,660 units recalled.
The recall affects multiple lot numbers, including Master Lot Number 516191 and various 30-pack and 90-pack lot numbers. Consumers can identify affected products by checking the lot numbers listed in the recall details, which include specific UDI numbers 733905577215, 733905615078, and 733905888472. The source document does not specify what consumers should do regarding this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
Johnson and Johnson Vision Care received a number of reports of a partially formed contact lens, which appears to the customer or consumer as visibly smaller in diameter, thicker/stiffer to the touch and more darkly tinted blue than the normal contact lens.
Reason for recall: Johnson and Johnson Vision Care received a number of reports of a partially formed contact lens, which appears to the customer or consumer as visibly smaller in diameter, thicker/stiffer to the touch and more darkly tinted blue than the normal contact lens. Distribution: Worldwide distribution: US (Nationwide) distribution to CA, CT, FL, GA, IA, IL, MA, MD, ME, MO, NC, NE, NH, NJ, NY, OH, PA, TN, TX, UT, and VA, Puerto Rico; and countries of: Canada, Barbados, Japan, and Korea. Quantity: 195,660 Total; 89,640 US & Puerto Rico, 106,020 OUS Lot/code info: Master Lot Number 516191. 90 Pack Lot Number (US, PR, Canada, Barbados) 5165915104 which contains 30 pack lot numbers: 5165910104, 5165910105, 5165910106, 5165910107, 5165910108, 5165910109. 90 Pack Lot Number (Japan) 5165915110 which contains 30 pack lot numbers: 5165910110, 5165910111, 5165910112. 90 Pack Lot Number (Korea and Japan) 5165915101 which contains 30 pack lot numbers: 5165910101, 5165910102, 5165910103. Unique Device Identifier (UDI): 733905577215, 733905615078, and 733905888472.
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.