Z-2469-2012 Class II Terminated
FDA device recall Z-2469-2012 was initiated by Linvatec Corp. dba ConMed Linvatec on July 1, 2011 and is designated Class II. Reason for recall: ConMed Linvatec recalled their 24k Arthroscopy Outflow/Suction Tubing Set (Product Number 24k100)because there is a possibility that the product may have a breach in the Tyvek seal that could potentia… The recall status is terminated (terminated July 25, 2013). Affected quantity: 30064 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 3, 2012
- Initiation Date
- July 1, 2011
- Termination Date
- July 25, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 30064 units
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution--USA (nationwide) including the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, LA, MA, MD, MI, MN, MO, NC, NE, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, WA ,WI and Hawaii., and the countries of Australia Canada, China, Switzerland, Germany, Czech Republic, Denmark, Egypt, Spain, France, South Africa, United Kingdom, Israel, Italy, Netherlands, New Zealand, Poland, Portugal, Russia and Saudi Arabia.