Apple Medical Corporation Fischer Cone Biopsy Excisor - Lg - Shallow Model: 900-155 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Fischer Cone Biopsy Excisor - Lg - Shallow Model: 900-155
Brand
Apple Medical Corporation
Lot Codes / Batch Numbers
Lot Numbers: D201710, A2005, D205004, D218913, D229701, D304806, D307910, D316307, H213D, J073C, L153Q, A134B
Products Sold
Lot Numbers: D201710, A2005, D205004, D218913, D229701, D304806, D307910, D316307, H213D, J073C, L153Q, A134B
Apple Medical Corporation is recalling Fischer Cone Biopsy Excisor - Lg - Shallow Model: 900-155 due to Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be r. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.
Recommended Action
Per FDA guidance
Apple Medical Corporation issued letters dated March 21, 2006 to direct accounts and distributors via US Mail. Distributors are requested to sub-recall. Product is to be returned to the firm and destroyed.
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