Kamra Corneal Inlay Aci 7000 (2016-02-11)
KAMRA Corneal Inlay ACI 7000 Recall The KAMRA Corneal Inlay ACI 7000, a medical device implanted in the eye to improve vision, was recalled across Canada. The device had a manufacturing defect that could cause it to separate or break during implantation or use. This recall affected all units of this product distributed in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-02-22
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4dbfd4be-114a-4f92-941a-da25055ce571