FDA Enforcement
Class II
Terminated
Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm 14MTWX x 12.5 cm
Recall: Z-0817-2019
·
Reported February 13, 2019
Enforcement
- Recall Number
- Z-0817-2019
- Event ID
- 81968
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Angiotech (Manan Medical Products, Inc.)
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- February 13, 2019
- Initiation Date
- December 18, 2018
- Classification Date
- February 7, 2019
- Termination Date
- August 23, 2020
- Address
- 241 W Palatine Rd, Wheeling, IL, 60090-5824, United States
Description
Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm 14MTWX x 12.5 cm
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 Info
Model Number BMNJ-MEC-1110, Lot Number LHT1
Distribution
Worldwide distribution - US Nationwide in the states of New Jersey, and countries of Mexico and South Korea.
Quantity
500 units