Z-2986-2020 Class II Terminated

Recalled by Sorin Group Italia S.r.l. — Saluggia, N/A

FDA device recall Z-2986-2020 was initiated by Sorin Group Italia S.r.l. on July 29, 2020 and is designated Class II. Reason for recall: LivaNova received complaints indicating the impossibility to collapse Perceval valve during procedure. The Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Pe… The recall status is terminated (terminated May 17, 2021). Affected quantity: 102 kits.

Recall Details

Product Type
Devices
Report Date
September 30, 2020
Initiation Date
July 29, 2020
Termination Date
May 17, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
102 kits

Product Description

Perceval Single Use Accessory Kit, Size S, REF: ICV1349, Sterile EO, Rx Only, CE, UDI: 8022057015211 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant, allowing the Perceval implantation.

Reason for Recall

LivaNova received complaints indicating the impossibility to collapse Perceval valve during procedure. The Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant, allowing the Perceval implantation. The issue is relevant to specific lots of Dual Collapser size S/M.

Distribution Pattern

US Nationwide distribution including in the states of CA, FL, ID, ME, MN, MO, MS, NC, SD, OH, OR, PA, SD, TN, TX, VA, WA, WI and the countries of Canada, Japan, Germany, Netherland, Switzerland, Sweden, UK, Spain, Italy, France, Belgium, Finland, Greece, Slovenia, Malta, Poland, Romania, Croatia, Hungary, Serbia, Australia, Israel, Georgia, Iran, Kuwait, Oman, Quatar, Singapore, Thailand, Taiwan, Russia, South Africa.

Code Information

Kit Lots: 2002200196, 2001300339, 2002130159