RecallRadar

FDA Device recall Z-0244-2026

Model Number 40KWFX, Mobile X-ray system

On 2025-10-29 the FDA classified a Class II recall of Model Number 40KWFX, Mobile X-ray system by Sedecal, citing sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, cle….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0244-2026
ClassificationClass II
Statusongoing
Initiated2025-06-10
Published2025-10-29
Last updated2026-09-13 11:57 UTC
CompanySedecal
DistributionCA, IL, NJ

Product

Model Number 40KWFX, Mobile X-ray system

Reason

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Identifiers

code_info
UDI/DI 08436046002166, Serial Numbers: G71453, G70953, G70930, G70537, G70757, G70797, G70275, G71257, G71983, G71975,…UDI/DI 08436046002166, Serial Numbers: G71453, G70953, G70930, G70537, G70757, G70797, G70275, G71257, G71983, G71975, G71467, G69702, G71440, G71329, G70244, G70955, G71462, G71320, G71451, G71466, G71335, G71446, G65260, G70951, G70814, G70931, G70942, G71991, G70261, G72080, G69697, G71978, G70938, G70247, G70250, G70947, G69706, G78917, G70943, G71343, G71345, G71346, G71258, G70527, G69551, G71442, G71977, G71987, G72083, G70242, G72111, G70256, G70806, G71339, G69547.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0244-2026%22

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