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Kamra Corneal Inlay ACI 7000 (2013-11-08)
- Starting date:
- November 8, 2013
- Posting date:
- June 12, 2014
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-39979
Recalled products
- Kamra Corneal Inlay ACI 7000
Reason
Acufocus is aware of reports of some cases this device being used in eyes containing Kamra Inlays. This notice is to update customers on ophthalmic procedures with a Kamra Inlay in situ.
Affected products
A. Kamra Corneal Inlay ACI 7000
Lot or serial number
All lots
Model or catalog number
- ACI 7000
Companies
- Manufacturer
-
Acufocus Inc.
32 Discovery, Suite 200
Irvine
92618
California
UNITED STATES