CLASS II Device recall · Reported 24 Dec 2014 · FDA Enforcement Report

Pkg, Axial Handle, W/ratchet, Insulated Shaft recalled

Stryker Endoscopy is recalling Pkg, Axial Handle, W/ratchet, Insulated Shaft, distributed nationwide in the US. The recall was initiated on 17 Nov 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes41811 140622 140726 140727 140729 342723 345252 544042 544043 644785 645845 645850 645852 645854 648085 06CON06065 744231 744232 745522 746745 840675 842159 842161 842197 842207 846841 846842 846844 846845 846847 846848 846849 846850 846851 846853 846855 942926 942943 942944 942945 942946 942947 942950 942951 942953 942954 942960 942964 943554 1044584 1044800 1045871 1046151 1046152 1046159 1046162 1046165 1140204 1140205 1140659 1140660 1140662 1142190 1142191 1143092 1143093 1143436 1143437 1144693 1144694 1144696 1145106 1145400 1145478 1146161 1146982 1240188 1240189 1241117 1241949 1242400 1243129 1243584 1243585 1244442 1244882 1246186 1246187 1340352 1340493 1340494 1341007 1341164 1341880 1342685 1342858 1344252 1344707 1440353 1442562 1443626 544043 645847

Quantity recalled180,573 units total

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0625-2015
FDA event ID: 69838
Recalling firm: Stryker Endoscopy, San Jose, CA
Classification: Class II
Status: Terminated
Recall initiated: 17 Nov 2014
FDA classified: 17 Dec 2014
Reported: 24 Dec 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Sterility
Device type: Heart & Vascular Devices

Timeline

17 Nov 2014	Recall initiated by company
17 Dec 2014	Classified by FDA	+30 days
24 Dec 2014	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

PKG, AXIAL HANDLE, W/RATCHET, INSULATED SHAFT, P/N 0250080235. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

Where it was distributed

Worldwide Distribution - USA (nationwide) and Internationally to Algeria, Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, France, Germany, Greece, Guam, Guatemala, India, Italy, Japan, Jordan, Kuwait, Latin America, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Saudi Arabia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, and Venezuela.

Nationwide Puerto Rico

Questions about this recall

Is Pkg, Axial Handle, W/ratchet, Insulated Shaft recalled?

Yes. Stryker Endoscopy recalled Pkg, Axial Handle, W/ratchet, Insulated Shaft on 17 Nov 2014. The recall is Class II and its status is Terminated. Recall number Z-0625-2015.

Why was it recalled?

Which lots are affected?

41811 140622 140726 140727 140729 342723 345252 544042 544043 644785 645845 645850 645852 645854 648085 06CON06065 744231 744232 745522 746745 840675 842159 842161 842197 842207 846841 846842 846844 846845 846847 846848 846849 846850 846851 846853 846855 942926 942943 942944 942945 942946 942947 942950 942951 942953 942954 942960 942964 943554 1044584 1044800 1045871 1046151 1046152 1046159 1046162 1046165 1140204 1140205 1140659 1140660 1140662 1142190 1142191 1143092 1143093 1143436 1143437 1144693 1144694 1144696 1145106 1145400 1145478 1146161 1146982 1240188 1240189 1241117 1241949 1242400 1243129 1243584 1243585 1244442 1244882 1246186 1246187 1340352 1340493 1340494 1341007 1341164 1341880 1342685 1342858 1344252 1344707 1440353 1442562 1443626 544043 645847

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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