RecallDepth

VNS Therapy SENTIVA Generator Model # 1000 Labeling 26-0009-6800 Model 1000 Generator Sample Labels 26-0009-9600 Patient s Manual for Depression 26-0009-9500 Patient s Manual for Epilepsy 76-0000-5000 VNS Therapy System Physician s Manual (refer to Attachment 1)

Company
Livanova Usa, Inc.
Recall Initiated
August 13, 2019
Terminated
May 18, 2022
Recall Number
Z-1118-2020
Quantity
6 generators
Firm Location
Houston, TX

Reason for Recall

Firm identified a subset of its generators that were sterilized one additional sterilization cycle, which does not meet the firm's quality specifications.

Distribution

US: FL, GA, KS, MO, and UT. No OUS distribution

Lot / Code Info

Model Serial No. UDI Model 1000 204460 01054250257504051119080317201205212044609910-0011-6102  Model 1000 183960 01054250257504051119080217200912211839609910-0011-6102  Model 1000 194980 01054250257504051119080217201030211949809910-0011-6102  Model 1000 204700 01054250257504051119080217201205212047009910-0011-6102  Model 1000 206720 01054250257504051119080317201219212067209910-0011-6102  Model 1000 213290 01054250257504051119080517210108212132909910-0011-6102

Root Cause

Process control

Action Taken

On 08/13/2019, the firm contacted via telephone hospitals/facilities of the immediate need to remove and replace the affected devices. Reference Firm email communication dated 1/27/2020. On 08/30/2019, prescribing physicians were telephone call with a follow-up email recommending replacement of the generators during an already planned or unrelated lead replacement surgery.

More recalls by Livanova Usa, Inc.

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