RecallRadar

FDA Device recall Z-0277-2026

Model Number SM-40HF-B-D-C

On 2025-10-29 the FDA classified a Class II recall of Model Number SM-40HF-B-D-C 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-0277-2026
ClassificationClass II
Statusongoing
Initiated2025-06-10
Published2025-10-29
Last updated2026-09-13 11:57 UTC
CompanySedecal
DistributionCA, IL, NJ

Product

Model Number SM-40HF-B-D-C; 40KW, 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 08436046001510, Serial Numbers: G65281, G60407, G65682, G64582, G64789, G70752, G65384, G65418, G67250, G68470,…UDI/DI 08436046001510, Serial Numbers: G65281, G60407, G65682, G64582, G64789, G70752, G65384, G65418, G67250, G68470, G70521, G70524, G70913, G70914, G65166, G63507, G64205, G64842, G71447, G65175, G65382, G64793, G64798, G40226, G72434, G65554, G67230, G37280, G65174, G65558, 15033R, G64271, G64713, G64849, G65168, G71272, G71309, G65284, G72955, G65043, G70919, G72429, G72789, G70928, G72776, G72766, G63409, G63418, G64893, G66907, G65588, G65402, G73096, G73131, G71269, G71750, G71762, G71267, G71727, G71732, G71745, G71755, G71761, G66892, G65275, G70922, G73154, G64505, G65744, G73033, G73134, G64941, G63489, G65036, G64256, G72976, G73092, G73145, G64196, G64945, G72412, G73074, G65414, G71726, G71743, G64807, G66872, G67257, G40208, G64885, G38391, G39467, G39818, G65408, G70748, G37108, G6715, G67232, G71277, G71286, G64604, G37406, G40004, G63223, G63224, G63232, G61711, G71271, G71302, G72790, G64500, G65269, G65692, G65290, G65691, G66862, G65283, G64189, G70744, G64812, G

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-0277-2026%22

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