Micromedics, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1817-2017)

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:

Nordson Micromedics FibriJet Endoscopic Catheter Introducer, Catalog Number SA-3445. Sterilized using Ethylene Oxide

Product Classification:

Class II

Date Initiated: October 20, 2016

Date Posted: April 19, 2017

Recall Number: Z-1817-2017

Event ID: 75890

Reason for Recall:

The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package integrity may be compromised which may affect sterility assurance.

Status: Terminated

Product Quantity: 273 units

Code Information:

Lot Number: 163010 Expiration date: June 2021

Distribution Pattern:

AL, CA, FL, MS, NC, NJ, NY, TN, and TX. Outside the US: Israel

Voluntary or Mandated:

Voluntary: Firm initiated