Midmark Corporation recalls Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate,
Midmark recalls IQvitals Zone blood pressure monitors with model numbers 1-200-03300 and 1-200-0330 that may give inaccurate blood pressure readings when using the Linear Deflation Method. Affected units were sold between 2020 and 2023.
Lower-risk recall
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
What happened, in plain English
Midmark is recalling IQvitals Zone blood pressure monitors that may provide inaccurate readings when using the Linear Deflation Method. This could lead to incorrect health assessments if the device is relied upon for medical decisions. Read more at govinfonow.com/recall/1292564-midmark-iqvitals-zone-blood-pressure-device-inaccurate-readings-with-linear.
Source Summary by GovInfoNow · govinfonow.com/recall/1292564-midmark-iqvitals-zone-blood-pressure-device-inaccurate-readings-with-linear · Published October 6, 2026 · Updated October 6, 2026 · FDA enforcement record: FDA #Z-3218-2026
Cite this page
“Midmark IQvitals Zone Blood Pressure Device: Inaccurate Readings with Linear Deflation Method.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1292564-midmark-iqvitals-zone-blood-pressure-device-inaccurate-readings-with-linear. Based on FDA recall #Z-3218-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3218-2026%22&limit=1).
Why it’s dangerous
The device may give inaccurate blood pressure readings when the Linear Deflation Method is used. This method involves slowly releasing air from the cuff to measure pressure, which can cause errors in the readings.
Who’s affected
Adults and pediatric patients who own or use the IQvitals Zone blood pressure monitor with model numbers 1-200-03300 or 1-200-0330 are affected. Those using the device for medical monitoring are most at risk.
How to tell if you have this one
Check for model numbers 1-200-03300 or 1-200-0330 on the device. The product was sold between 2020 and 2023 and includes specific serial numbers listed in the recall notice.
- Brand
Midmark- Category
Medical device
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-3217-2026 | Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-0320 with Kit Number: 4-000-0622; Model No: 1-200-0320; UDI-DI: 00841709105791; Kit No: 4-000-0622; UDI-DI: 00841709105876; Kit Serial Number: V2900924; Zone Serial Number: V2899738 | 1 units |
| Z-3218-2026 | Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-03300 with Kit Number: 4-000-0624; Model No: 1-200-0330; UDI-DI: 00841709105807; Kit No: 4-000-0624; UDI-DI: 00841709105883; Kit Serial Number: V2842901 V2841713 V2841724 V2842133 V2842105 V2841750 V2841701 V2842116 V2842081 V2842097 V2866067 V2871822 V2871211 V2871204 V2871817 V2881636 V2878754 V2878741 V2878759 V2879975 V2879979 V2879564 V2880715 V2880713 V2881270 V2880698 V2880711 V2879544 V2881253 V2882161 V2881704 V2882141 V2881259 V2881258 V2881698 V2881677 V2881684 V2879566 V2882146 V2879551 V2877649 V2877655 V2877673 V2880021 V2878308 V2878306 V2878734 V2877678 V2878299 V2878294 V2880023 V2875958 V2875328 V2877119 V2877065 V2874409 V2877114 V2874415 V2875941 V2875331 V2876441 V2876423 V2874794 V2874786 V2877057 V2877131 V2873684 V2876410 V2876449 V2873677 V2876455 V2888858 V2896346 V2897752 V2896689 V2897157 V2895863 V2899478 V2898923 V2896355 V2898561 V2896708 V2897134 V2896352 V2898573 V2895879 V2899469 V2895878 V2899455 V2898942 V2898200 V2896720 V2898188 V2898192 V2898563 V2898930 V2897759 V2897764 V2897128 V2914273 V2914285 V2914304 V2915752 V2918767 V2915294 V2917735 V2920483 V2919267 V2918780 V2918750 V2920462 V2920473 V2919288 V2919879 V2917216 V2915308 V2918123 V2914243 V2918146 V2916948 V2917204 V2914807 V2915283 V2915770 V2916220 V2915298 V2914786 V2920109 V2919859 V2919892 V2919298 V2919281 V2917241 V2917747 V2918173 V2917727 V2916228 V2916203 V2915760 V2914792 V2914817 V2915785 V2916239 V2916929 V2918139 V2917715 V2916785 V2914256 V2928158 V2928139 V2928117 V2928129 V2928148; Zone Serial Number: L1187570 V2839311 V2840480 V2841440 V2841442 V2839313 V2838889 V2841435 V2839314 V2841486 V2846602 V2845499 V2845501 V2866711 V2845500 V2881442 V2878467 V2878461 V2877997 V2879643 V2879586 V2878874 V2880188 V2880175 V2877380 V2880218 V2880199 V2878949 V2880749 V2881496 V2881388 V2881510 V2877999 V2878828 V2881403 V2881416 V2881439 V2878838 V2881509 V2878895 V2877353 V2877331 V2876771 V2879576 V2877377 V2877386 V2878004 V2876760 V2877894 V2877903 V2879624 V2875578 V2875077 V2876138 V2876486 V2872543 V2876578 V2870918 V2875573 V2875048 V2876034 V2876051 V2874521 V2874524 V2876622 V2876761 V2870921 V2876137 V2872026 V2872523 V2872034 V2886993 V2896054 V2897368 V2895831 V2896886 V2895538 V2895546 V2896839 V2895832 V2896877 V2896521 V2896903 V2896028 V2896862 V2895519 V2895829 V2895526 V2896025 V2895830 V2897374 V2896517 V2897832 V2897835 V2896871 V2896508 V2897367 V2897380 V2896912 V2913819 V2913772 V2883155 V2915485 V2917114 V2915045 V2917451 V2917113 V2918943 V2917115 V2918374 V2920114 V2916371 V2918949 V2919507 V2917112 V2889736 V2917916 V2913975 V2917913 V2915498 V2916373 V2914494 V2915051 V2915063 V2915903 V2915048 V2914512 V2919533 V2919471 V2919479 V2918944 V2918929 V2883461 V2917431 V2917912 V2917463 V2915904 V2915902 V2915505 V2914503 V2914493 V2915504 V2915901 V2916370 V2917915 V2917453 V2916368 V2913974 V2925899 V2926403 V2925236 V2926955 V2918377 | 153 units |
| Z-3219-2026 | Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-0350 with Kit Number: 4-000-0722; Model No: 1-200-0350; UDI-DI: 00841709105821; Kit No: 4-000-0722; UDI-DI: 00841709105906; Kit Serial Number: V2866143 V2866111 V2866124 V2864892 V2864113 V2864444 V2864120 V2864449 V2864894 V2866626 V2866636 V2871280 V2870561 V2869170 V2870570 V2869930 V2874364 V2897744 V2900961 V2900947; Zone Serial Number: V2864929 V2865546 V2864921 V2864495 V2796056 V2864174 V2858651 V2864142 V2873819 V2866216 V2866187 V2870249 V2870090 V2867500 V2866707 V2869394 V2873111 V2886635 V2873150 V2886126 | 20 units |
| Z-3220-2026 | Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-0360 with Kit Number: 4-000-0724; Model No: 1-200-0360; UDI-DI: 00841709105838; Kit No: 4-000-0724; UDI-DI: 00841709105913; Kit Serial Number: V2788703 V2788046 V2788016 V2788712 V2789302 V2789846 V2789830 V2789837 V2789808 V2789303 V2789304 V2811103 V2811112 V2862288 V2862275 V2869139 V2866577 V2867451 V2869599 V2868801 V2869154 V2868545 V2866984 V2869980 V2869969 V2868130 V2867433 V2868182 V2924525 V2924566 V2924559 V2924539 V2927525; Zone Serial Number: V2788322 V2787552 V2787555 V2788321 V2788905 V2789498 V2787554 V2789488 V2789499 V2788922 V2787553 V2807891 V2807893 V2837260 V2859050 V2868888 V2862992 V2866942 V2868893 V2868239 V2868840 V2868222 V2866940 V2868892 V2869397 V2867491 V2866963 V2868051 V2923639 V2922999 V2922998 V2923640 V2927201 | 33 units |
What to do — step by step
Check Device Model
Look for model numbers 1-200-03300 or 1-200-0330 on the device.
Contact Manufacturer
Reach out to Midmark Corporation for assistance with the recall.
Questions people ask
Why is this device being recalled?
The device may provide inaccurate blood pressure readings when using the Linear Deflation Method, which could lead to incorrect health assessments.
What model numbers are affected?
Model numbers 1-200-03300 and 1-200-0330 are affected.
How can I tell if my device is affected?
Check for model numbers 1-200-03300 or 1-200-0330 on the device. The product was sold between 2020 and 2023.
Contact Midmark
We’ve drafted a message you can send Midmark to request your refund or repair — edit it as you like.
Subject: Recall Z-3218-2026 — Midmark Midmark Hello, I own a Midmark that is covered by recall Z-3218-2026 from Midmark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-3218-2026 (August 21, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3218-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.