InfuTronix LLC: Medical Device Recall in 2019 - (Recall #: Z-2055-2019)

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:

Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a container to a patient through a needle or a catheter.

Product Classification:

Class II

Date Initiated: May 28, 2019

Date Posted: July 31, 2019

Recall Number: Z-2055-2019

Event ID: 82997

Reason for Recall:

Potential for tube leakage

Status: Terminated

Product Quantity: 10,800 units

Code Information:

1) Lot # 1805002, Exp Date 06/10/2021, 2) Lot # 1712005, Exp Date 12/19/2020, 3) Lot # 1710012, Exp Date 10/22/2020, 4) Lot # 1901003, Exp Date 01/07/2022

Distribution Pattern:

US distribution in the state of MA

Voluntary or Mandated:

Voluntary: Firm initiated