Becton Dickinson and Company BD Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson & Company (BD) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson & Company (BD)
Brand
Becton Dickinson and Company
Lot Codes / Batch Numbers
All serial numbers
Products Sold
All serial numbers
Becton Dickinson and Company is recalling BD Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson & Company (BD) due to Microkeratome blade may stop oscillating and transverse the eye causing injury to the cornea. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Microkeratome blade may stop oscillating and transverse the eye causing injury to the cornea
Recommended Action
Per FDA guidance
BD Medical notified customers by Advisory Letter dated 8/09/07, advising users to return heads and bearing cartridges for replacement of the o-ring.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026