Class 2 Device Recall PKG, NEEDLE HOLDER, CURVED LEFT,

• Date Initiated by Firm: November 17, 2014
• Date Posted: December 12, 2014
• Recall Status: Terminated on July 17, 2015
• Recall Number: Z-0690-2015
• Recall Event ID: 69838
• Product Classification: Endoscope and/or accessories - Product Code KOG
• Product: 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.
• 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
• Recalling Firm/ Manufacturer: Stryker Endoscopy; 5900 Optical Ct; San Jose CA 95138-1400
• For Additional Information Contact: 408-754-2000
• Manufacturer 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
• FDA Determined Cause: Error in labeling
• Action: Stryker Endoscopy sent an Urgent Device Correction letter dated November 17, 2014, to affected customers. The letter informed the customers of the potential hazards and actions required. Customers were instructed to discard any old Instructions for Use for their Laparoscopic Manual Instruments and Accessories. Download the new Instuctions for Use (IFU1000-401-070 Revision J) from the URL link below: www.stryker.com/IFU1000401070 Customers were instructed to complete and sign the enclosed "Acknowledgement of Receipt" form and email them to endorecall@stryker.com or fax to (408) 855-6314. Customers with questions were instructed to contact Stryker Endoscopy at 408-855-6238 or via email at endorecall@stryker.com. For questions regarding this recall call 408-754-2000.
• Quantity in Commerce: 180,573 units total
• Distribution: 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.

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.