FDA recall Z-2523-2023

Aomori Olympus Co., Ltd. · Class II · device

Product

Reusable distal attachments Models: MH-462, MH-463, MH-464, MH-465, MH-466, MH-483, MH-587, MH-588(US), MH-589, MH-590, MH-591, MH-592, MH-593, MH-594, MH-595, MH-596, MH-597, MH-598, MAJ-289, MAJ-290, MAJ-291, MAJ-292, MAJ-293, MAJ-294, MAJ-295, MAJ-296, MAJ-297, MAJ-663, MAJ-664, MAJ-665, MAJ-666

Reason for recall

The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which exceeds the permissible exposure level calculated according to ISO 10993-17: 2002

Distribution

US Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2023-07-27
Report date
2023-09-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
Kuroishi, N/A, Japan

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2523-2023