Z-2056-2013 Class II Terminated
FDA device recall Z-2056-2013 was initiated by Integra Limited on July 17, 2013 and is designated Class II. Reason for recall: As a result of complaint investigations it was identified that there is a potential that the Leyla Ball Joint Clamp (R2383) may not provide the level of stability needed to maintain retraction in all … The recall status is terminated (terminated October 1, 2014). Affected quantity: 65.
Recall Details
- Product Type
- Devices
- Report Date
- September 4, 2013
- Initiation Date
- July 17, 2013
- Termination Date
- October 1, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 65
Product Description
Integra Leyla Ball Joint Clamp, also as included in Leyla Table Mounting Hardware. The Leyla Retraction System, as part of the Ruggles brand of instruments is intended for use as a self-retaining retractor which is a self-locking device used to hold the edges of a wound open during neurosurgery.
Reason for Recall
As a result of complaint investigations it was identified that there is a potential that the Leyla Ball Joint Clamp (R2383) may not provide the level of stability needed to maintain retraction in all cases.
Distribution Pattern
Worldwide Distribution - USA including Puerto Rico and the states of AZ, CA, FL, GA, IL, IN, KY, MA, MI, MS, NE, NM, NY, OH, PA, TN, TX, UT, VA, WA, WI and WV., and the countries of Spain, Singapore, South Africa, Canada, Libya,Pakistan and Cayman Islands.
Code Information
Catalog Number R2383 and as a component of catalog number R2385, including all lot numbers date codes going back to January 2006.