FDA Device recall Z-0072-2024

LFS Flat screen support arm systems without surgical lamp for models Aurora series, Aurora 2 series, Aurora 3 series, Aurora 4 series, Auro…

FDA Device
Class II
ongoing
Published 2023-10-11

On 2023-10-11 the FDA classified a Class II recall of LFS Flat screen support arm systems without surgical lamp for models Aurora series, Aurora 2 series, Aurora 3 series, Aurora 4 series, Auro… by Dkk Dai Ichi Shomei, citing the stopper block on the LFS bracket could be broken or missing. Without this stopper block, the flat screen attached to the LFS flat screen system can rotate beyond the original….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0072-2024
Classification	Class II
Status	ongoing
Initiated	2023-08-23
Published	2023-10-11
Last updated	2026-09-13 11:56 UTC
Company	Dkk Dai Ichi Shomei
Distribution	MI

Product

LFS Flat screen support arm systems without surgical lamp for models Aurora series, Aurora 2 series, Aurora 3 series, Aurora 4 series, Aurora Astro series, Stellar XL, and Stellar series, LFS Flat Screen Support Arm Model Numbers

Reason

The stopper block on the LFS bracket could be broken or missing. Without this stopper block, the flat screen attached to the LFS flat screen system can rotate beyond the original angle limit and it could cause excessive force to be given to the spring shaft of the LFS bracket. Due to the excessive force given to the spring shaft, the spring shaft could break and shear off.

Identifiers

code_info	Serial Numbers: RA000006, RA000007, RA000008, RA000009, RA000010, RA000244, RA000245, RA000246, RA000247, RA000248, RA0… Serial Numbers: RA000006, RA000007, RA000008, RA000009, RA000010, RA000244, RA000245, RA000246, RA000247, RA000248, RA000359, RA000360, RA000361, RA000362, RA000363, RA000364, RA000365, RA000366, RA000367, RA000368, RA000391, RA000393, RA000408, RA000410, RA000412, RA000414, RA000416, RA000418, RA000374, RA000459, RA000648, RA000712, RA000714, RA000716, RA000718, RA000720, RA000722, RA000724, RA000726, RA000751, RA000752, RA000753, RA000754, RA000755, RA000756, RA000757, RA000905, RA000907, RA000909, RA000911, RA000916, RA000918, RA000920, RA000922, RA000924, RA000926, RA001136, RA001138, RA001144, RA001145, RA001146, RA001147, RA001148, RA001197, RA001198, RA001199, RA001200, RA001201, RA001202, RA001203, RA001204, RA001205, RA001206, RA001189, RA001190, RA001244, RA001246, RA001252, RA001253, RA001254, RA001255, RA001256, RA001257, RA001287, RA001288, RA001289, RA001290, RA001291, RA001292, RA001299, RA001300, RA001345, RA001347, RA001374, RA001376, RA001377, RA001378, RA001379, RA00

code_info

Serial Numbers: RA000006, RA000007, RA000008, RA000009, RA000010, RA000244, RA000245, RA000246, RA000247, RA000248, RA0…

Serial Numbers: RA000006, RA000007, RA000008, RA000009, RA000010, RA000244, RA000245, RA000246, RA000247, RA000248, RA000359, RA000360, RA000361, RA000362, RA000363, RA000364, RA000365, RA000366, RA000367, RA000368, RA000391, RA000393, RA000408, RA000410, RA000412, RA000414, RA000416, RA000418, RA000374, RA000459, RA000648, RA000712, RA000714, RA000716, RA000718, RA000720, RA000722, RA000724, RA000726, RA000751, RA000752, RA000753, RA000754, RA000755, RA000756, RA000757, RA000905, RA000907, RA000909, RA000911, RA000916, RA000918, RA000920, RA000922, RA000924, RA000926, RA001136, RA001138, RA001144, RA001145, RA001146, RA001147, RA001148, RA001197, RA001198, RA001199, RA001200, RA001201, RA001202, RA001203, RA001204, RA001205, RA001206, RA001189, RA001190, RA001244, RA001246, RA001252, RA001253, RA001254, RA001255, RA001256, RA001257, RA001287, RA001288, RA001289, RA001290, RA001291, RA001292, RA001299, RA001300, RA001345, RA001347, RA001374, RA001376, RA001377, RA001378, RA001379, RA00

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-0072-2024%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.