Source: FDA | Recall date: 11/05/2025
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Affected product: Alcon Laboratories, Inc.: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000250 UNITY 27+DS HYPERVIT 30K VIT PROBE 8065753168
Brand: alcon research llc
Hazard: Due to incomplete seals in the pouch which provide the sterile barrier.
Official identifiers
Track your baby products and get automatic recall alerts when something may affect your family.
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