CLASS II Device recall · Reported 24 Dec 2014 · FDA Enforcement Report
Pkg, Rotating Handle, W/ratchet, Insulated Shaft recalled
Stryker Endoscopy is recalling Pkg, Rotating 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
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-0621-2015
- 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, ROTATING HANDLE, W/RATCHET, INSULATED SHAFT, P/N 0250080230. 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.
Questions about this recall
Why was it recalled?
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
Which lots are affected?
40727 41812 42276 42321 43396 140312 143267 245172 246071 246923 247037 340652 340653 440289 441514 441892 443352 443353 444984 444985 51299 0543138D 0543898D 0640771D 0641429D 0644144D 0646013D 0647316D 0647549D 0740185D 0744066D 0744695D 0746332D 0840071D 0840907D 0842105D 0843936D 0844813D 0846982D 0846986D 0847650D 0847661D 0847671D 92509 0941061D 0941604D 0941726D 0944836D 0945121D 0945472D 0945725D 0945884D 0945983D 1040247D 1040397D 1040426D 1040985D 1042094D 1042466D 1042503D 1042504D 1042940D 1042942D 1044541D 1045186D 1045983D 1046856D 1140701D 1141744D 1142005D 1143438D 1143439D 1144077D 1144676D 1144677D 1145548D 1145549D 1146121D 1240550D 1242235D 1243162 1243162D 1243163 1243596 1340609 1340610 1340610D 1341875 1341876 1342868 1342868D 1342869 1345090 1345090D 1345799 1440293 181299 511298 521298
Where was it sold?
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.
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
100 other products · FDA event 69838This product is part of a recall event; the main page for the event is Pkg, Bipolar Forceps, Fenestrated recalled by Stryker Endoscopy.
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