Acuvue Oasys for Astigmatism Contact Lenses Recalled for Package Integrity Failure
Johnson & Johnson Vision Care is recalling specific Acuvue Oasys for Astigmatism contact lenses due to a package integrity failure found during routine testing.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text explicitly states the issue was a package integrity failure found during routine testing with no reported illnesses or injuries, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Johnson & Johnson Vision Care, Inc. is recalling 150 units of ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. The affected product is identified by Lot no. B00NKM0G, Base Curve 8.6, and Refractive Power -3.00D-1.25/90. The lenses were distributed nationwide in the United States.
The recall was initiated after a package integrity failure was observed during routine shift package integrity testing at an external re-packager. The source text does not specify the nature of the failure or report any illnesses or injuries associated with the product.
Consumers who possess the affected contact lenses should stop using them and contact Johnson & Johnson Vision Care for further instructions or a refund.
The recalled product
- Product
- ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.
- Manufacturer
- Johnson & Johnson Vision Care, Inc.
- Category
- Medical Device — Contact Lenses
- Hazard
- Affected units
- 150
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot no. B00NKM0G. Base Curve 8.6
- Refractive Power -3.00D-1.25/90.
Distribution
Distributed nationwide across the United States.
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