FDA Device recall Z-0259-2020

Various products which were contract sterilized

FDA Device
Class II
ongoing
Published 2019-11-06

On 2019-11-06 the FDA classified a Class II recall of Various products which were contract sterilized by Anewmed, citing the contract sterilizer did not have adequate packaging data to support the 2-year shelf life.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0259-2020
Classification	Class II
Status	ongoing
Initiated	2019-05-23
Published	2019-11-06
Last updated	2026-09-13 11:55 UTC
Company	Anewmed
Distribution	US

Product

Various products which were contract sterilized.

Reason

The contract sterilizer did not have adequate packaging data to support the 2-year shelf life.

Identifiers

code_info	Product Number (Lot Code): 1. G26862 (W3915653); 2. 8065751801 (15027297X-2015-06); 3. E7924 (HD1206703)… Product Number (Lot Code): 1. G26862 (W3915653); 2. 8065751801 (15027297X-2015-06); 3. E7924 (HD1206703); 4. MCFK64 (MBKY190); 5. PCB502090 (16105672, 17525844); 6. PCB602090 (17766962, 17716501, 17505067, 17465154, 17339717, 17191941, 16536005, 15473410, 15441264, 16685888); 7. PCB702090 (16722293); 8. 277-10-50 (12094017); 9. 420024 (73B1500332); 10. 160636 (1202143, 1109213), 11. 160656 (1208163); 12. 7210424 (50506601); 13. AD750-KE40 (169-16), AD750-KE35 (182-16); 14. AD750-KE30 (102-16); 15. AD750-KE35 ( 118-16); 16. 614-481 (648221); 17. 76353200M (208992282, 207180152, 206969148, 206110579); 18. ASHA4250-01 (2004847); 19. GN1000 (9592565); 20. GN1500 (9916746); 21. SK200 (9577286); 22. GN2000 (9909194); 23. 9-AVP2-014 (1204040241); 24. 9-AVP2-016 (1201055704); 25. 401814RMC (35227834); 26. EICA5872-01 (1035512, 1049334, 1046764, 1050636); 27. 101

code_info

Product Number (Lot Code): 1. G26862 (W3915653); 2. 8065751801 (15027297X-2015-06); 3. E7924 (HD1206703)…

Product Number (Lot Code): 1. G26862 (W3915653); 2. 8065751801 (15027297X-2015-06); 3. E7924 (HD1206703); 4. MCFK64 (MBKY190); 5. PCB502090 (16105672, 17525844); 6. PCB602090 (17766962, 17716501, 17505067, 17465154, 17339717, 17191941, 16536005, 15473410, 15441264, 16685888); 7. PCB702090 (16722293); 8. 277-10-50 (12094017); 9. 420024 (73B1500332); 10. 160636 (1202143, 1109213), 11. 160656 (1208163); 12. 7210424 (50506601); 13. AD750-KE40 (169-16), AD750-KE35 (182-16); 14. AD750-KE30 (102-16); 15. AD750-KE35 ( 118-16); 16. 614-481 (648221); 17. 76353200M (208992282, 207180152, 206969148, 206110579); 18. ASHA4250-01 (2004847); 19. GN1000 (9592565); 20. GN1500 (9916746); 21. SK200 (9577286); 22. GN2000 (9909194); 23. 9-AVP2-014 (1204040241); 24. 9-AVP2-016 (1201055704); 25. 401814RMC (35227834); 26. EICA5872-01 (1035512, 1049334, 1046764, 1050636); 27. 101

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0259-2020%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.