Medical Device Technologies, Inc. Angiotech, Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for use during Bone Marrow Biopsy. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Angiotech, Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for use during Bone Marrow Biopsy.
Brand
Medical Device Technologies, Inc.
Lot Codes / Batch Numbers
Lot Number 81371NGF and 81081MRM.
Products Sold
Lot Number 81371NGF and 81081MRM.
Medical Device Technologies, Inc. is recalling Angiotech, Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for due to Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.
Recommended Action
Per FDA guidance
Each consignee was notified of recall by letter on 07/16/2008 . The letter described the problem and indicated the corrective action to be taken. A Customer Acknowledgment Form with request to fax form to firm's QA Dept was provided. Contact Medical Device Technologies, Inc., Quality Assurance Department at 1.352.338.0440, ext 350 and 353 for assistance.
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