Z-2549-2018 Class II Ongoing
FDA device recall Z-2549-2018 was initiated by Guangzhou Improve Medical Instruments Co., Ltd. on September 22, 2017 and is designated Class II. Reason for recall: Leaks complaints. The recall status is ongoing. Affected quantity: 200,000.
Recall Details
- Product Type
- Devices
- Report Date
- August 1, 2018
- Initiation Date
- September 22, 2017
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 200,000
Product Description
Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
Reason for Recall
Leaks complaints.
Distribution Pattern
Kansas
Code Information
Serial Number 102030178 Lots #: 160809