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PKG, NEEDLE HOLDER, CURVED LEFT, P/N 0250080341. Laparoscopic Manual Instruments are intended fo...

FDA Device Recall #Z-0690-2015 — Class II — November 17, 2014

Recall Summary

Recall Number Z-0690-2015
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, NEEDLE HOLDER, CURVED LEFT, P/N 0250080341. 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

247810 244921 340067 343901 544103 644138 741292 744238 940159 940784 942133 942134 942279 942685 943256 943444 943446 943740 943859 943860 944295 944829 944925 945726 1040111 1040424 1041099 1041277 1041381 1042093 1042502 1042938 1045028 1045477 1045934 1046110 1046399 1046929 1140657 1141381 1142928 1143002 1143269 1144233 1144241 1144347 1144627 1144657 1145409 1145678 1145965 1145970 1146360 1146655 1147045 1240113 1240952 1241423 1241810 1241811 1241939 1242460 1244168 1244186 1244529 1245023 1245443 1246066 1341576 1341578 1341579 1343713 1344281 1344463 1440469

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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