Terumo Cardiovascular Systems Corporation: Medical Device Recall in 2019 - (Recall #: Z-0966-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222

Product Classification:

Class II

Date Initiated: December 20, 2018

Date Posted: March 6, 2019

Recall Number: Z-0966-2019

Event ID: 82019

Reason for Recall:

Presence of natural rubber latex is not declared in the label

Status: Terminated

Product Quantity: 12 packs

Code Information:

Lot Numbers: V A30

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated