Z-1149-2017Class II

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

Name: Z-1149-2017 QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes...
Creator: Stryker Leibinger GmbH & Co. KG
Published: 2017-01-03
License: https://open.fda.gov/license/

Stryker Leibinger GmbH & Co. KG / initiated 2017-01-03 / Terminated / root cause: labeling and UDI

FDA source

Stryker Leibinger GmbH & Co. KG began a recall of 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... on 2017-01-03. FDA classified it as Class II and gives the reason as "An incorrect sterility status on the label, non-sterile products labeled as sterile". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-1149-2017
Classification: Class II
Status: Terminated
Initiated: 2017-01-03
Posted: 2017-02-08
Terminated: 2017-07-27
Recalling firm: Stryker Leibinger GmbH & Co. KG
Product: 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 code: GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
Reason for recall: An incorrect sterility status on the label, non-sterile products labeled as sterile
Root cause tag: labeling and UDI
FDA root cause: Labeling mix-ups
Action: Stryker sent an " URGENT MEDICAL DEVICE RECALL" notifications dated January 3, 2017, to the affected customers. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, instructions for returning affected product, and instructions for responding to the formal recall notification. Please report any adverse events or product quality problems to Stryker CMF Customer Service: 1 (800) 962-6558.
Quantity in commerce: 619
Distribution: Worldwide Distribution - USA (nationwide) Distribution and to the countries of : Australia, Canada, Chile, Spain, South Africa and Taiwan.
Product codes and lots: 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

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1149-2017
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1149-2017	Class II	Terminated	Voluntary: Firm initiated	2017-02-15	2017-02-08
Z-1150-2017	Class II	Terminated	Voluntary: Firm initiated	2017-02-15	2017-02-08

Product code GCY

K833586Class ITls Bulb Drainage SystemPorex Medical / cleared 1984-01-30

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)