Medical Device Recall: Z-0031-2022

FDA Recalls dataset · Firm: NOX MEDICAL Keldnaholt Reykjavik Iceland · Status: Terminated

Recall Action Class: N/A Date Initiated: 2021-09-07 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0031-2022.

Recall Res Number
Z-0031-2022
Recalling Firm / Manufacturer
FEI Number
3007389703
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2021-09-07
Date Posted
N/A
Date Terminated
2023-05-01
Product Code
MNR
Event Number
88673
Product Quantity
128 units
Product Description Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.

Reason for Recall Error in the device firmware results in the inaccurate detection of device position.

Action Details Written notification letter titled, "URGENT: Medical Device Recall" was sent to all consignees on 09/07/2021. The letter instructs the consignee to follow the following instructions: "Further distribution or use of the affected devices should cease immediately. Devices should be quarantined pending device firmware update, per the instructions below. Due to the potential of inaccurate position-related reporting of TST, TRT, AHI and REI; studies performed with the affected T3s devices should be reanalyzed to determine if this has clinical impact on the patient diagnoses. A Nox Medical technical representative will contact you within 5 business days to schedule a remote session (via videoconference or other means) to upgrade the device firmware. Nox Medical requests that you formally acknowledge receipt of this notice and return the attached Customer / Distributor - Acknowledgement and Receipt Form (Attachment 1). This recall notice needs to be passed on to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. If any affected devices which were in your possession (indicated in Attachment 2: Product Distribution and Information Table) have been transferred, please indicate this and provide as much detail as possible in the Acknowledgement and Receipt Form (Attachment 1)."

Distribution Pattern US Nationwide distribution in the states of OH, IL, GA, IA, CA, PA, NM, MI, SD.

Code Information / Serial Numbers Catalog Number: 561111; UDI: (01)15694311111443; Serial Numbers: 300106423, 300106426, 300106420, 300106419, 300106422, 300106427, 300106425, 300106424, 300106421, 300106477, 300106485, 300106783, 300106806, 300106841, 300106843 , 300106846, 300106848, 300106852, 300106853, 300106857, 300106862, 300106881, 300106882, 300106883, 300106884, 300106885, 300106886, 300106888, 300106889, 300106890, 300106894, 300106897, 300106912, 300107004, 300106385, 300106396, 300106397, 300106407, 300106413, 300106414, 300106399, 300106415, 300106416, 300106475, 300106476, 300106483, 300106486, 300106494, 300106534, 300106537, 300106538, 300106544, 300106545, 300106547, 300106548, 300106552, 300106648, 300106658, 300106675, 300106677, 300106678, 300106684, 300106754, 300106772, 300106775, 300106807, 300106809, 300106810, 300106812, 300106839, 300106842, 300106849, 300106855, 300106868, 300106891, 300106892, 300106899, 300106909, 300106926, 300106951, 300107003, 300106398, 300106481, 300106542, 300106546, 300106782, 300106910, 300106400, 300106535, 300106536, 300106808, 300106950, 300106469, 300106470, 300106869, 300106854, 300106478, 300106805, 300106811, 300106840, 300106850, 300106856, 300106859, 300106887, 300106893, 300106895, 300106896, 300106898, 300107005, 300106776, 300106781, 300106789, 300106788, 300106833, 300106549, 300106543, 300106557, 300106540, 300106533, 300106556, 300106555, 300106901, 300106786, 300106553, 300106784, 300106541, 300106777, 300106774

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