3/8X3/8X3/8 Y CONN, STRL REF/ GTIN for Insert Label:EC2105S/ 00803622129285
This recall has been terminated (originally issued April 24, 2020).
- Company
- Livanova Usa Inc.
- Recall Initiated
- April 24, 2020
- Terminated
- February 17, 2022
- Recall Number
- Z-2459-2020
- Quantity
- 220 units
- Firm Location
- Arvada, CO
- Official Source
- View on FDA website ↗
Reason for Recall
XXX
Distribution
US - AK, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WV OUS- Spain (Hospital de Barsuto, Bilbao, Spain)
Lot / Code Info
LOT2004300008
Root Cause
Packaging process control
Action Taken
The firm sent an URGENT MEDICAL DEVICE REMOVAL letter to affected customers on 04/24/2020. The purpose of this medical device correction is to: 1. Advise the customers of the present issue and not to use the affected devices; 2. Providing information to the user on product disposal or return and replacement; 3. Inform affected customers that LivaNova will coordinate replacement for the unused products.