MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2022 - (Recall #: Z-0088-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

VENCLOSE, VENCLOSE PROCEDURE PACK, 7VM, REF VC-PPH-67A. Cardiovascular procedure convenience kit.

Product Classification:

Class II

Date Initiated: September 1, 2022

Date Posted: October 19, 2022

Recall Number: Z-0088-2023

Event ID: 90889

Reason for Recall:

Impacted Venclose Procedure Packs contain a 12cm introducer/sheath component, either component #128626 - SET INTRO 7FX12CM FITS 0.018 or component #137339 - SET INTRO 6.5FX12CM FITS 0.018, instead of a 7cm introducer/sheath, component #137340 - SET INTRO 6.5FX7CM FITS 0.018

Status: Terminated

Product Quantity: 1760 kits

Code Information:

UDI/DI 40193489423090, lot number 22EBV345, exp. 08/31/2024; UDI/DI 10193489423099, lot number 22FBF358, exp. 08/31/2024

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated