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PKG, ROTATING HANDLE, W/RATCHET, INSULATED SHAFT, P/N 0250080230. Laparoscopic Manual Instrumen...

FDA Device Recall #Z-0621-2015 — Class II — November 17, 2014

Recall Summary

Recall Number Z-0621-2015
Classification Class II — Moderate risk
Date Initiated November 17, 2014
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Stryker Endoscopy
Location San Jose, CA
Product Type Devices
Quantity 180,573 units total

Product Description

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.

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

Distribution Pattern

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.

Lot / Code Information

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

Other Recalls from Stryker Endoscopy

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Z-1566-2016 Class II PneumoSure XL High Flow Insufflator and Pneumo... Mar 28, 2016
Z-1831-2015 Class II SERFAS 90 degree Energy Probe, Part Number 279-... Jun 3, 2015
Z-0631-2015 Class II PKG, PENNINGTON FORCEPS, P/N 0250080242. Lapa... Nov 17, 2014
Z-0646-2015 Class II PKG, ENDO METZENBAUM SCISSORS, CURVED, P/N 0250... Nov 17, 2014
Z-0679-2015 Class II PKG, ALLIGATOR FORCEPS, P/N 0250080316. Laparo... Nov 17, 2014

Frequently Asked Questions

Sterility recalls for medical devices vary in severity. If you have already had a procedure using a potentially non-sterile device, contact your healthcare provider immediately — you may need monitoring for signs of infection. Symptoms to watch for include fever, redness or swelling at the surgical site, unusual pain, or discharge. For devices that have not yet been used, they should be quarantined and returned to the manufacturer per the recall notice. Non-sterile implants can cause serious infections; early detection and treatment are critical.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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