Midmark recalls
4 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Midmark and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-09-30FDA-DeviceClass IIMidmark IQvitals Zone recalled for inaccurate blood pressure readings
Midmark's IQvitals Zone vital signs monitor may provide inaccurate blood pressure readings when using the Linear Deflation Method. The issue affects a limited number of units (33 total) distributed nationwide. No injuries have been reported.
- 2026-09-30FDA-DeviceClass IIMidmark IQvitals Zone recalled for inaccurate blood pressure readings
Midmark Corporation's IQvitals Zone vital signs monitor may produce inaccurate blood pressure readings when using the Linear Deflation Method. The issue affects a limited number of units with specific serial numbers distributed nationwide. No injuries have been reported.
- 2026-09-30FDA-DeviceClass IIMidmark IQvitals Zone recalled for inaccurate blood pressure readings
Midmark Corporation's IQvitals Zone vital signs monitor may produce inaccurate blood pressure readings when using the Linear Deflation Method. The device measures blood pressure, pulse, temperature, and oxygen levels for adult and pediatric patients. A limited number of units with specific serial numbers are affected.
- 2026-09-30FDA-DeviceClass IIMidmark IQvitals Zone recalled for inaccurate blood pressure
Midmark Corporation's IQvitals Zone vital signs monitor may display inaccurate blood pressure readings when using the Linear Deflation Method. This affects Model 1-200-0320 with Kit 4-000-0622. The device measures blood pressure, pulse, temperature, and oxygen saturation for adult and pediatric patients.
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