Myelotec, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2779-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels

Product Classification:

Class II

Date Initiated: March 2, 2017

Date Posted: August 9, 2017

Recall Number: Z-2779-2017

Event ID: 77508

Reason for Recall:

Obstructed/blocked port from defective VGC Access Port Body component.

Status: Ongoing

Product Quantity: 2980 units

Code Information:

Lot No. 4123/MY33613, 4250/MY06614, 4279/MY06614, 4305/MY10814, 4331/MY13914, and 4331/MY25214

Distribution Pattern:

Worldwide Distribution - US Distribution to the states of : CA, FL, KY, MN, and NJ ., and to the countries of : Brazil, Iran, Kuwait, Malaysia, Singapore, South Korea, Taiwan, and Turkey

Voluntary or Mandated:

Voluntary: Firm initiated