FDA Device recall Z-1241-2022
Nester Embolization Microcoil RPN GPN MWCE-18-5-2-NESTER G52733 MWCE-18-5-3-NESTER G52734 MWCE-18-7-3-NESTER-01 G47338 MWCE-18-7-2-NESTER-0…
- FDA Device
- Class II
- ongoing
- Published 2022-06-15
On 2022-06-15 the FDA classified a Class II recall of Nester Embolization Microcoil RPN GPN MWCE-18-5-2-NESTER G52733 MWCE-18-5-3-NESTER G52734 MWCE-18-7-3-NESTER-01 G47338 MWCE-18-7-2-NESTER-0… by Cook, citing the loading cartridges included with these devices may contain a small, unintended, stainless-steel cannula.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1241-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-05-05 |
| Published | 2022-06-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cook |
| Distribution | US |
Product
Nester Embolization Microcoil RPN GPN MWCE-18-5-2-NESTER G52733 MWCE-18-5-3-NESTER G52734 MWCE-18-7-3-NESTER-01 G47338 MWCE-18-7-2-NESTER-01 G47337 MWCE-18-7-5-NESTER-01 G47340 MWCE-18-3-2-NESTER G52731 MWCE-18-7-8-NESTER-01 G47342 MWCE-18-7-8-NESTER G52739 MWCE-18-7-5-NESTER G23521 MWCE-18-3-3-NESTER G52732 MWCE-18-5-3-NESTER-01 G47334 MWCE-18-7-6-NESTER G52738 MWCE-18-7-6-NESTER-01 G47341 MWCE-18-3-3-NESTER-01 G47332 MWCE-18-7-4-NESTER G52737 MWCE-18-7-3-NESTER G52736 MWCE-18-3-2-NESTER-01 G47331 MWCE-18-5-2-NESTER-01 G47333 MWCE-18-2-2-NESTER-01 G47344 MWCE-18-5-5-NESTER-01 G47335 MWCE-18-7-2-NESTER G52735 MWCE-18-7-4-NESTER-01 G47339 MWCE-18-7-10-NESTER G52741 MWCE-18-5-5-NESTER G23520
Reason
The loading cartridges included with these devices may contain a small, unintended, stainless-steel cannula.
Identifiers
| code_info | Lots: 14445809 NS14440413 14438720 NS14533529 NS14531987 NS14512935 NS14531991 NS14531985 NS14531989 NS14531990 NS1453…Lots: 14445809 NS14440413 14438720 NS14533529 NS14531987 NS14512935 NS14531991 NS14531985 NS14531989 NS14531990 NS14531993 NS14531994 14230667 14219518 14228061 14232591 14233388 14233393 14280197 14299971 14239561 14239563 14240096 14227837 14231033 14231052 14232846 14318778 14343805 NS14318613 NS14345341 14325852 14366728 NS14341560 NS14345338 NS14345796 14317075 14366729 14395251 14446172 14452759 14461634 14542803 14542804 14542805 NS14533531 14502814 14233390 14223991 14280196 14299968 14299969 14228357 14240093 14240095 14240097 14242960 14280193 14280194 NS14242956 NS14267436 NS14285103 NS14285105 NS14285113 NS14285116 NS14285118 14343806 14343808 14401670 14560261 14242333 14242961 14244909 14230666 14231051 14231480 14236762 14239564 14240094 14242899 14280195 14244951 14340480 14343008 14363296 NS14329321 14363792 14371377 14392159 14557484 14558691 14560262 14244907 14239562 14303167 14303168 14233392 14244908 14387092 14391580 14368792 14394030 14404724 14411527 14411533 |
|---|
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-1241-2022%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.