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Medical Device

Convenience kits CATARACT PACK DYNJ59881A

Recall date: 2026-09-23 · Source: FDA_DEVICE
Product
Convenience kits CATARACT PACK DYNJ59881A
Reason for recall
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
Units affected
336
Description
Convenience kits CATARACT PACK DYNJ59881A
View official recall notice →