Cook Inc.: Medical Device Recall in 2016 - (Recall #: Z-0733-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous Catheter Tray Cook Spectrum Minocycline/Rifampin Impregnated Triple Lumen Central Venous Catheter Tray

Product Classification:

Class II

Date Initiated: November 28, 2016

Date Posted: December 21, 2016

Recall Number: Z-0733-2017

Event ID: 75793

Reason for Recall:

Cook Medical has received reports of the trays containing the incorrect needle, which in some cases could result in the inability to pass a wire guide through the needle. Potential adverse events that may occur as a result of utilizing needles of incorrect size include delay in treatment, which could be critical in an emergent situation. There have been no reports of illness or injury associated with this issue.

Status: Terminated

Product Quantity: 99 units

Code Information:

catalog number: C-UDLMY-401J-ABRM-HC-FST Lot 6498570 catalog number: C-UTLMY-501J-ABRM-HC-FST Lot 6501835 Exp date 9/30/2018

Distribution Pattern:

AZ CA DC GA IL LA MN MS NC NV NY OK PA TN TX WI

Voluntary or Mandated:

Voluntary: Firm initiated