FDA Device recall Z-1644-2022

EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System

FDA Device
Class II
ongoing
Published 2022-09-07

On 2022-09-07 the FDA classified a Class II recall of EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System by Medtronic, citing update to IFU provides a manual deployment workaround method to help mitigate potential harms related to partial stent deployment.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1644-2022
Classification	Class II
Status	ongoing
Initiated	2022-07-14
Published	2022-09-07
Last updated	2026-09-13 11:56 UTC
Company	Medtronic
Distribution	n/a

Product

EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System

Reason

Update to IFU provides a manual deployment workaround method to help mitigate potential harms related to partial stent deployment.

Identifiers

code_info	All Lot codes: 1) Model Number EVX35-08-060-120, GTIN 00763000052355; 2) Model Number EVX35-05-020-080, GTIN 007630000… All Lot codes: 1) Model Number EVX35-08-060-120, GTIN 00763000052355; 2) Model Number EVX35-05-020-080, GTIN 00763000051655; 3) Model Number EVX35-05-020-120, GTIN 00763000051662; 4) Model Number EVX35-05-020-150, GTIN 00763000051679; 5) Model Number EVX35-05-040-080, GTIN 00763000051686; 6) Model Number EVX35-05-040-120, GTIN 00763000051693; 7) Model Number EVX35-05-040-150, GTIN 00763000051709; 8) Model Number EVX35-05-060-080, GTIN 00763000051716; 9) Model Number EVX35-05-060-120, GTIN 00763000051723; 10) Model Number EVX35-05-060-150, GTIN 00763000051730; 11) Model Number EVX35-05-080-080, GTIN 00763000051747; 12) Model Number EVX35-05-080-120, GTIN 00763000051754; 13) Model Number EVX35-05-080-150, GTIN 00763000051761; 14) Model Number EVX35-05-100-080, GTIN 00763000051778; 15) Model Number EVX35-05-100-120, GTIN 00763000051785; 16) Model Number EVX35-05-100-150, GTIN 00763000051792; 17) Model Number EVX35-05-120-080, GTIN 00763000051808; 18) Model Number EVX35-05

code_info

All Lot codes: 1) Model Number EVX35-08-060-120, GTIN 00763000052355; 2) Model Number EVX35-05-020-080, GTIN 007630000…

All Lot codes: 1) Model Number EVX35-08-060-120, GTIN 00763000052355; 2) Model Number EVX35-05-020-080, GTIN 00763000051655; 3) Model Number EVX35-05-020-120, GTIN 00763000051662; 4) Model Number EVX35-05-020-150, GTIN 00763000051679; 5) Model Number EVX35-05-040-080, GTIN 00763000051686; 6) Model Number EVX35-05-040-120, GTIN 00763000051693; 7) Model Number EVX35-05-040-150, GTIN 00763000051709; 8) Model Number EVX35-05-060-080, GTIN 00763000051716; 9) Model Number EVX35-05-060-120, GTIN 00763000051723; 10) Model Number EVX35-05-060-150, GTIN 00763000051730; 11) Model Number EVX35-05-080-080, GTIN 00763000051747; 12) Model Number EVX35-05-080-120, GTIN 00763000051754; 13) Model Number EVX35-05-080-150, GTIN 00763000051761; 14) Model Number EVX35-05-100-080, GTIN 00763000051778; 15) Model Number EVX35-05-100-120, GTIN 00763000051785; 16) Model Number EVX35-05-100-150, GTIN 00763000051792; 17) Model Number EVX35-05-120-080, GTIN 00763000051808; 18) Model Number EVX35-05

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1644-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.