Ebola IgX VP-40 Serum/Plasma/Blood Cassette, Catalog No. I-100 Materials Provided: 1. Test Device 2. Lancet 3. Alcohol pad. 4. Develop buffer tube contain buffer vial (0.3ml)
Recall
- Recall Number
- Z-1328-2015
- Event Number
- 70668
- Firm
- Lusys Laboratories, Inc.
- FEI Number
- 3004473533
- Product Code
- N/A
- Status
- Terminated
- Root Cause
- No Marketing Application
- Initiated
- March 13, 2015
- Posted
- April 9, 2015
- Terminated
- May 31, 2017
- Address
- 10054 Mesa Ridge Ct, Ste 118-120, San Diego, CA, 92121-2946
Description
Ebola IgX VP-40 Serum/Plasma/Blood Cassette, Catalog No. I-100 Materials Provided: 1. Test Device 2. Lancet 3. Alcohol pad. 4. Develop buffer tube contain buffer vial (0.3ml)
LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and prevent further use of these devices. The Ebola Virus One-Step Test Kits have not yet been cleared, approved or authorized by the FDA for diagnostics purposes.
LuSys Laboratories sent an Urgent Medical Device Recall letter dated March 13, 2015, to all affected customers informing them that the Ebola Virus One Step Test Kits are not approved by FDA for diagnostics purposes. The letter informs the customers of the problems identified and the actions to be taken. Customers were instructed to discontinue use and return the products to LuSys Laboratories. Customers are instructed to fax back the acknowledgement and Receipt Form to 1-858-866-1688. For questions regarding this recall call 858-546-0902.
Worldwide Distribution - US including CA and Internationally to Canada, Sierra Leone, and Denmark.
1,055 units