Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026
Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate,…
Midmark Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Midmark Corporation · 60 Vista Dr · Versailles, OH · 45380-9488
Is this the product you have?
- 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 Number1-200-03300
- with Kit Number4-000-0624
- Lot codes and dates
- Model No1-200-0330
- UDI-DI00841709105807
- Kit No4-000-0624
- UDI-DI00841709105883
- Kit Serial Number
153 of 153 codes
V2842901V2841713V2841724V2842133V2842105V2841750V2841701V2842116V2842081V2842097V2866067V2871822V2871211V2871204V2871817V2881636V2878754V2878741V2878759V2879975V2879979V2879564V2880715V2880713V2881270V2880698V2880711V2879544V2881253V2882161V2881704V2882141V2881259V2881258V2881698V2881677V2881684V2879566V2882146V2879551V2877649V2877655V2877673V2880021V2878308V2878306V2878734V2877678V2878299V2878294V2880023V2875958V2875328V2877119V2877065V2874409V2877114V2874415V2875941V2875331
- Zone Serial Number
153 of 153 codes
L1187570V2839311V2840480V2841440V2841442V2839313V2838889V2841435V2839314V2841486V2846602V2845499V2845501V2866711V2845500V2881442V2878467V2878461V2877997V2879643V2879586V2878874V2880188V2880175V2877380V2880218V2880199V2878949V2880749V2881496V2881388V2881510V2877999V2878828V2881403V2881416V2881439V2878838V2881509V2878895V2877353V2877331V2876771V2879576V2877377V2877386V2878004V2876760V2877894V2877903V2879624V2875578V2875077V2876138V2876486V2872543V2876578V2870918V2875573V2875048
- Amount recalled
- 153 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Midmark Corporation recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.