Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED Recalled by Philips North America LLC Due to Affected devices contain a Printed Circuit Assembly (PCA)...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America LLC directly.
Affected Products
Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED, Model 861304, HSI codeRev: E.03.063
Quantity: Total 96 units = 95 units (HS1 Onsite) and 1 unit (HS1 Home)
Why Was This Recalled?
Affected devices contain a Printed Circuit Assembly (PCA) that was not manufactured/repaired in accordance to quality standards.
Where Was This Sold?
This product was distributed to 13 states: CA, CT, FL, IL, MI, MS, MO, NJ, NY, TN, TX, WA, WI
About Philips North America LLC
Philips North America LLC has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report