Numed Inc: Medical Device Recall in 2018 - (Recall #: Z-0510-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for use in catheterization for angiography of cardiovascular vessels and I or chambers. It can be used for injection of contrast medium and pressure measurement in any chamber or vessel.

Product Classification:

Class II

Date Initiated: October 17, 2018

Date Posted: December 5, 2018

Recall Number: Z-0510-2019

Event ID: 81460

Reason for Recall:

Instructions for Use booklets were not included on the outer pouch

Status: Terminated

Product Quantity: 100 units

Code Information:

Lot numbers: 5MT-1264, 5MT-1265 Exp. Date: 2023-09-30 UDI: 04046964312700

Distribution Pattern:

US distribution in the state of PA

Voluntary or Mandated:

Voluntary: Firm initiated