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PKG, METZENBAUM SCISSORS, CURVED LONG, P/N 0250080265. Laparoscopic Manual Instruments are inte...

FDA Device Recall #Z-0644-2015 — Class II — November 17, 2014

Recall Summary

Recall Number Z-0644-2015
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

Product Description

PKG, METZENBAUM SCISSORS, CURVED LONG, P/N 0250080265. 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

140280 143823 244698 341493 443333 541776 545061 647416 744587 842092 844289 846109 846772 846819 941064 941065 941852 942140 943501 943549 944300 945744 945886 945977 1040098 1040413 1041057 1041621 1041992 1042086 1042240 1042475 1042685 1042695 1042698 1042714 1044482 1045035 1045373 1045641 1046199 1046595 1046933 1046934 1046943 1142155 1142668 1142897 1142910 1143132 1144208 1144398 1144492 1144940 1145080 1145798 1145971 1146839 1146933 1240119 1241514 1241515 1242921 1244191 1244534 1245445 1246192E 1246638 1246638E 1246650 1340099 1341584 1341585 1343125 1343402 1343402E 1343705 1344204 1344286 1344456 1344880 1345236 1345532 1345532E 1345605 1345605E 1346432 1346666 1440405 1440684 1442518 1443219 1443653 1443917

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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