Medical Device Technologies, Inc. Angiotech, Bone Marrow Aspiration Needle, Medical Device Technologies, Inc. Individual packaged in blister pack. Packaged 10 per box. Sterile. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Angiotech, Bone Marrow Aspiration Needle, Medical Device Technologies, Inc. Individual packaged in blister pack. Packaged 10 per box. Sterile.
Brand
Medical Device Technologies, Inc.
Lot Codes / Batch Numbers
Lot Number 81351NDR
Products Sold
Lot Number 81351NDR
Medical Device Technologies, Inc. is recalling Angiotech, Bone Marrow Aspiration Needle, Medical Device Technologies, Inc. Individual packaged in 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