FDA Enforcement
Class II
Ongoing
IUD Insertion Pack
Recall: Z-0127-2022
·
Reported October 27, 2021
Enforcement
- Recall Number
- Z-0127-2022
- Event ID
- 88656
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Stradis Medical, LLC dba Stradis Healthcare
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- October 27, 2021
- Initiation Date
- September 10, 2021
- Classification Date
- October 16, 2021
- Address
- 3025 Northwoods Pkwy, N/A, Peachtree Corners, GA, 30071-1524, United States
Description
IUD Insertion Pack
Reason
Firm unable to confirm that the tenaculum devices were produced in accordance with required design and manufacturing standards.
Code Info
Part Number: 618-034
Distribution
Distributed nationwide to VA, SC, CA, PA, MA, FL, TN, NJ, GA, AZ, IL, OH, OK, WA, NY, NV, MO, MD, IN, TX, CO, RI, NC, KY, MT, VI, GA, KS, MI, AK, ID, SD, UT and internationally to Canada.
Quantity
20 kits