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FDA (Device enforcement)Recalled 2023-08-23class ii

DKK Dai-Ichi Shomei Co., Ltd.: 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, a

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: US States: MI Quantity: 1211 units Lot/code info: 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, RA001380, RA001381, RA001382, RA001383, RA001384, RA001385, RA001386, RA001434, RA001435, RA001439, RA001469, RA001470, RA001471, RA001472, RA001473, RA001474, RA001475, RA001476, RA001479, RA001480, RA001503, RA001529, RA001553, RA001555, RA001572, RA001573, RA001574, RA001575, RA001585, RA001576, RA001588, RA001664, RA001665, RA001666, RA001668, RA001669, RA001670, RA001710, RA001711, RA001712, RA001713, RA001714, RA001729, RA001732, RA001708, RA001709, BM003066, BM003067, BM003068, BM003069, BM00

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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