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Recall Observatory FDA recall evidence

Device product

J Type Bone Marrow Needle 13ga x 10 cm- Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.

Z-0815-2019

December 18, 2018

Class II

Product summary

Firm
Angiotech (Manan Medical Products, Inc.)
Event
Event 81968
Status
Terminated
Classification
Class II
Quantity
1,260 units
Official record key
device-enforcement:Z-0815-2019

Official wording

Reason: Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line

Code information: Model Number IMKBMN-13R-10, Lot Numbers LF69, LFDA, LFL1

Distribution pattern: Worldwide distribution - US Nationwide in the states of New Jersey, and countries of Mexico and South Korea.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line