Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by Angiotech (Manan Medical Products, Inc.) Due to Argon Medical has identified an internal manufacturing issue...

Date: December 18, 2018
Company: Angiotech (Manan Medical Products, Inc.)
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Angiotech (Manan Medical Products, Inc.) directly.

Affected Products

Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm 14MTWX x 12.5 cm

Quantity: 500 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Angiotech (Manan Medical Products, Inc.)

Angiotech (Manan Medical Products, Inc.) has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report