FDA Device recall Z-0822-2013

Viterion TeleHealth Monitor Model Number V500

FDA Device
Class II
terminated
Published 2013-02-20

On 2013-02-20 the FDA classified a Class II recall of Viterion TeleHealth Monitor Model Number V500 by Viterion Telehealthcare, citing viterion telehealth monitors do not transmit "HI" (above the meter's measurable range) and "LO" (below the meter's measurable range) blood glucose readings from Bayer's Contour El….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0822-2013
Classification	Class II
Status	terminated
Initiated	2012-11-15
Published	2013-02-20
Last updated	2026-09-13 11:53 UTC
Company	Viterion Telehealthcare
Distribution	US

Product

Viterion TeleHealth Monitor Model Number V500; Product Codes 08832984 (US) and 02080468 (UK) - Physiological patient monitor (without arrhythmia detection or alarms). Viterion V100, V100-BGM and V500 Telehealth Monitors transfer medical information.

Reason

Viterion telehealth monitors do not transmit "HI" (above the meter's measurable range) and "LO" (below the meter's measurable range) blood glucose readings from Bayer's Contour Elite XL blood glucose meters, or from Roche's Accu-Chek Advantage 03 and 04 meters to healthcare professionals.

Identifiers

code_info	All units are affected. Serial Numbers A3303HA000201, A3303HA000202, A3303HA000203, A3303HA000204, A3303HA000205, A330… All units are affected. Serial Numbers A3303HA000201, A3303HA000202, A3303HA000203, A3303HA000204, A3303HA000205, A3304HA000206, A3304HA000207, A3304HA000208, A3304HA000209, A3304HA000210, A3305HA000211, A3305HA000212, A3305HA000213, A3305HA000214, A3305HA000215, A3306HA000216, A3306HA000217, A3306HA000218, A3306HA000219, A3306HA000220, A3310HA000221, A3310HA000222, A3310HA000223, A3310HA000224, A3310HA000225, A3404HA000226, A3404HA000227, A3404HA000228, A3404HA000229, A3404HA000230, A3404HA000231, A3404HA000232, A3404HA000233, A3404HA000234, A3404HA000235, A3404HA000236, A3404HA000237, A3404HA000238, A3404HA000239, A3404HA000240, A3404HA000241, A3404HA000242, A3404HA000243, A3404HA000244, A3404HA000245, A3404HA000246, A3404HA000247, A3404HA000248, A3404HA000249, A3404HA000250, A3602HA000252, A3602HA000253, A3602HA000254, A3602HA000255, A3602HA000256, A3602HA000257, A3602HA000258, A3602HA000259, A3602HA000260, A3602HA000261, A3602HA000262, A3602HA000263, A3602HA000264, A3602HA000265,

code_info

All units are affected. Serial Numbers A3303HA000201, A3303HA000202, A3303HA000203, A3303HA000204, A3303HA000205, A330…

All units are affected. Serial Numbers A3303HA000201, A3303HA000202, A3303HA000203, A3303HA000204, A3303HA000205, A3304HA000206, A3304HA000207, A3304HA000208, A3304HA000209, A3304HA000210, A3305HA000211, A3305HA000212, A3305HA000213, A3305HA000214, A3305HA000215, A3306HA000216, A3306HA000217, A3306HA000218, A3306HA000219, A3306HA000220, A3310HA000221, A3310HA000222, A3310HA000223, A3310HA000224, A3310HA000225, A3404HA000226, A3404HA000227, A3404HA000228, A3404HA000229, A3404HA000230, A3404HA000231, A3404HA000232, A3404HA000233, A3404HA000234, A3404HA000235, A3404HA000236, A3404HA000237, A3404HA000238, A3404HA000239, A3404HA000240, A3404HA000241, A3404HA000242, A3404HA000243, A3404HA000244, A3404HA000245, A3404HA000246, A3404HA000247, A3404HA000248, A3404HA000249, A3404HA000250, A3602HA000252, A3602HA000253, A3602HA000254, A3602HA000255, A3602HA000256, A3602HA000257, A3602HA000258, A3602HA000259, A3602HA000260, A3602HA000261, A3602HA000262, A3602HA000263, A3602HA000264, A3602HA000265,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0822-2013%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.