CareFusion 303, Inc.: Medical Device Recall in 2017 - (Recall #: Z-3030-2017)

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:

VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.

Product Classification:

Class II

Date Initiated: June 30, 2017

Date Posted: August 23, 2017

Recall Number: Z-3030-2017

Event ID: 77696

Reason for Recall:

Punctures in blister packaging that was detected during the packaging process.

Status: Terminated

Product Quantity: 1,546,800 units

Code Information:

Lot No. 1470303001, 1570314802, 1470303002, 1570317701, 1470304601, 1570317702, 1470306602, 1570317703, 1470306301, 1570317704, 1470306602, 1570322001, 1470311301, 1660771501, 1470306301, 1470311302, 1470314801

Distribution Pattern:

Worldwide Distribution in the states of : CO, IL, IN, MD, MI, NY, OH, & TX. and foreign countries of: Australia, New Zealand, & Japan.

Voluntary or Mandated:

Voluntary: Firm initiated