Device recalls

VOCSN Multi-Function Ventilators: VOCSN+Pro (V+O+C+S+N+Pro, English), REF: PRT-00490-001; V+Pro (V+Pro, English), REF: PRT-01185-000, PRT-0…

Ventec Life Systems, Inc. · Multi-Function Ventilators were serviced using incorrect parts which have the potential to cause unexpected shutdown, or when using an active circuit could res…

Open, ClassifiedComponent change controlZ-1196-2025
Open FDA's page for this record
Cfres ID
212111
Product res number
Z-1196-2025
Event date initiated
2025-02-03
Event date posted
2025-02-26
Recall status
Open, Classified
Res event number
96136
Product code
CBK
Product description
VOCSN Multi-Function Ventilators: VOCSN+Pro (V+O+C+S+N+Pro, English), REF: PRT-00490-001; V+Pro (V+Pro, English), REF: PRT-01185-000, PRT-01185-002
Firm FEI number
3013095415
Recalling firm
Ventec Life Systems, Inc.
Address 1
22002 26th Ave Se
City
Bothell
State
WA
Postal code
98021-4903
Additional info contact
425-686-1722
Root cause description
Component change control
Product quantity
30
Distribution pattern
US distribution in CA, NY, and MO.
Code info

REF/UDI-DI/Serial Numbers: PRT-00490-001/00855573007792/123627, 121892, 119639; PRT-01185-000/00855573007877/5038421, 116700, 117933, 5038112, 5038619, 5038717, 5038953, 5039086, 5039091, 5039361, 5039499, 5039503, 5039541, 5039636, 5039938, 5040019, 5040640, 5040762, 5041060, 5041078, 5041534, 5042558, 117344, 118464, 118509, 5039387; PRT-01185-002/00850018761154/5037655

Reason for recall

Multi-Function Ventilators were serviced using incorrect parts which have the potential to cause unexpected shutdown, or when using an active circuit could result in inaccurate tidal volume monitor, not triggering on patient efforts, less inspiratory volume, less inspiratory pressure, and less PEEP delivered.

Action

On 02/03/2025, recall notices were sent to Durable Medical Equipment Distributors asking them to do the following: Clinical Action: Follow internal procedures to transfer the patient to an alternative source of ventilation, if available. If no other ventilation method is available, you may continue to use the affected product adhering to the guidelines below, while you await device correction by firm Service personnel: 1. Use only when the patient is actively monitored to ensure timely response to a potential malfunction. 2. Operate the ventilator as defined in the Instructions for Use and promptly respond to all alarms activated by the ventilator. 3. Use external monitors (e.g. SpO2) and set the alarm thresholds appropriately for the patient. 4. Connect the ventilator to an external monitoring system, wherever possible. Also, Durable Medical Equipment Distributors are asked to acknowledge they forwarded the recall notice, and that they contacted the users to which the devices were provided, advised them of the recall and action instructions within accompanying Recall Notification Letter including how to have the devices repaired. Complete and return the acknowledgement form via email to Ventec-Recall@reacthealth.com For any questions contact the firm at at 844-MYVOCSN (844-698-6276), Monday through Friday between 8:00 a.m. - 5:00 p.m. PDT.

K numbers
K162877
Harmonized identifiers (openFDA)
Device name
Ventilator, Continuous, Facility Use
Medical specialty description
Anesthesiology
Regulation number
868.5895
Device class
2
K number
K173973, K872466, K083122, K252663, K060862, K093416, K820132, K913972, K243767, K023289, K983981, K905234, K092847, K842876, K981971, K852771, K010793, K924930, K820746, K062793, K072885, K982174, K021112, K813254, K253647, K030515, K894426, K092135, K181166, K862604, K241943, K820220, K862025, K910847, K003770, K980208, K941308, K881482, K052863, K884389 +465 more
Registration number
3010882708, 3030446844, 3018094310, 3014631252, 3029906224, 9680661, 3006087789, 3049813765, 3013154126, 3032026475, 3038562397, 8010939, 9615827, 1314417, 9611500, 3000143502, 3017520736, 1922553, 3002797442, 3003477135, 3001400310, 2112020, 3016450067, 3010817335, 3009156722, 3016618143, 3011205710, 3031369651, 3044156918, 3010834934, 3009609218, 2134715, 2221819, 3025936435, 2025816, 9617566, 1924066, 8020893, 3030733800, 8021084 +91 more
FEI number
3010882708, 3030446844, 3018094310, 3014631252, 3002807992, 3029906224, 3003952420, 3006087789, 3001237338, 3049813765, 3013154126, 3032026475, 3038562397, 1314417, 3003007937, 3000143502, 3017520736, 1922553, 3002797442, 3000957797, 3001400310, 2112020, 3003477135, 3016450067, 3010817335, 3009156722, 3002924544, 3016618143, 3011205710, 3031369651, 3044156918, 3010834934, 3009609218, 3003244771, 2221819, 3025936435, 2025816, 3002807626, 1924066, 1000115734 +91 more
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