Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067A
Reported: October 20, 2021 Initiated: February 9, 2021 #Z-0081-2022
Product Description
Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067A
Reason for Recall
Customers were not notified of previous recalls associated with various defibrillator models.
Details
- Recalling Firm
- Philips North America LLC
- Units Affected
- 15 units
- Distribution
- U.S.: CA, CT, FL, GA, IN, MI, MO, NJ, NY, OH, TX, and WA. International distribution in the countries of Australia, Canada, France, Germany, Japan, Norway, Switzerland.
- Location
- Bothell, WA
Frequently Asked Questions
What product was recalled? ▼
Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067A. Recalled by Philips North America LLC. Units affected: 15 units.
Why was this product recalled? ▼
Customers were not notified of previous recalls associated with various defibrillator models.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 20, 2021. Severity: Moderate. Recall number: Z-0081-2022.
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