Stryker Leibinger GmbH & Co. KG: Medical Device Recall in 2017 - (Recall #: Z-1149-2017)

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:

QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System

Product Classification:

Class II

Date Initiated: January 3, 2017

Date Posted: February 15, 2017

Recall Number: Z-1149-2017

Event ID: 76146

Reason for Recall:

An incorrect sterility status on the label, non-sterile products labeled as sterile

Status: Terminated

Product Quantity: 619

Code Information:

Part # 6630 QUINTUBE Monitor Pack Lots- M1305008, M1305009, M1305010, M1305011, M1309004, M1309005, M1309006, M1309007, M1309008, M1309009, M1309010, M1607009, M1607010, T1309003 Part # 6649 SPG Bulb Drain System, 4mm Flat w/Center Holes Lot - M1508003

Distribution Pattern:

Worldwide Distribution - USA (nationwide) Distribution and to the countries of : Australia, Canada, Chile, Spain, South Africa and Taiwan.

Voluntary or Mandated:

Voluntary: Firm initiated