FDA Enforcement
Class II
Terminated
Wilson Implantation System Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
Recall: Z-1611-2016
·
Reported May 11, 2016
Enforcement
- Recall Number
- Z-1611-2016
- Event ID
- 73318
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Applied Medical Technology Inc
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- May 11, 2016
- Initiation Date
- February 17, 2016
- Classification Date
- May 4, 2016
- Termination Date
- October 27, 2016
- Address
- 8000 Katherine Blvd, Brecksville, OH, 44141-4202, United States
Description
Wilson Implantation System Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
Reason
The firm received a complaint of an open pouch which breaches the sterilization validation.
Code Info
Part #: TLC5042-M
Distribution
Product was shipped to the following states: AL, AR, AZ, CA, CT, FL, GA, IA, IN, KS, KY, MA, MD, MI, MN, MO, NC, NE, NH, NJ, OH, PA, SC, TN,TX, UT, VA & WI. Product was also shipped to the following countries: Austria, Denmark, Germany, Italy, Japan, Norway, Spain, Sweden, Switzerland & United Kingdom.
Quantity
1,100 units