Argon Medical Devices, Inc: Medical Device Recall in 2017 - (Recall #: Z-1195-2017)

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:

T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN; T-LOK BONE MARROW BIOPSY NEEDLE 11G x 4 EXT CAN Intended for the purpose of harvesting bone and/or bone marrow specimens

Product Classification:

Class II

Date Initiated: January 18, 2017

Date Posted: February 22, 2017

Recall Number: Z-1195-2017

Event ID: 76292

Reason for Recall:

The recalling firm received a complaint from one of their customers of a potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.

Status: Terminated

Product Quantity: 772 boxes

Code Information:

lots: 11157523, 11158179, 11158180, 11159101, 11159729

Distribution Pattern:

Worldwide Distribution - US (nationwide) and Internationally to Switzerland, Canada, Australia, New Zealand, Ecuador, Colombia, and Japan.

Voluntary or Mandated:

Voluntary: Firm initiated