Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates could not be validated by the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Synergetics Inc directly.
Affected Products
BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)
Quantity: 116 units
Why Was This Recalled?
Sterilization certificates could not be validated by the supplier
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Synergetics Inc
Synergetics Inc has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report