Pennsylvania recalls
3,600 federal recalls affecting Pennsylvania in the last 12 months - 384 Pennsylvania-specific plus 3,216 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue Patient Monitor MX100. Product Number: 867033.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue Multi-Measurement Module X3. Product Number: 867030.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue Multi Measurement Server X2. Product Number: M3002A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP90. Product Number: M8010A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP80. Product Number: M8008A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP70. Product Number: M8007A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP60. Product Number: M8005A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP50. Product Number: M8004A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP40. Product Number: M8003A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP30. Product Number: M8002A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP20. Product Number: M8001A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP5. Product Number: M8105A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DevicePhilipsClass IINationwideIntelliVue MP2. Product Number: M8102A.
Potential issue where the IntelliVue monitors did not alarm.
- 2025-12-10FDA-DeviceFresenius KabiClass IINationwideIvenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.
Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.
- 2025-12-10FDA-DeviceBaxterClass IINationwideWelch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff.
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.
- 2025-12-10FDA-DeviceGet TestedClass IINationwide8 in 1 STI Test Kit
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwide3 in 1 STI Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwide2 in 1 Trichomonas / Gardnerella Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideSerotonin Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwidePollen Allergy Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwidePet Allergy Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideMelatonin Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideIron Deficiency Test (ferritin)
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideIodine Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideHeavy Metals Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideFood Intolerance Test Small
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideFood Intolerance Test Medium
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideFood Intolerance Test Large
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideEstrogen & Progesterone Test
Distribution without premarket approval/clearance.
- 2025-12-10FDA-DeviceGet TestedClass IINationwideAllergy test Small
Distribution without premarket approval/clearance.
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