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.
Action Details
On February 11, 2021, Philips issued a "Urgent - Safety Notification" to affected consignees via certified Mail. In addition to notifying consignees that may have been omitted from notification of one or more recalls, Philips asked affected consignees to take
1. To acknowledge receipt of this notification, please complete and return the Customer Reply Form by email or by fax by February 15, 2021.
Email to: ECR.Recall.Response@Philips.com
Or, Fax: 1 (833) 371-1011
2. A Philips representative will reach out to you to help you identify any affected AED.
3. After it has been confirmed that you have an affected AED and a replacement Philips AED has been sent to you, please return the affected AED to Philips using the shipping label to be provided.
4. The affected AED may remain in service until you receive a replacement Philips AED.
5. Philips will exchange affected devices with a replacement Philips AED free of charge.
6. If you need any further information or support concerning this issue, please contact Philips at 1 (800) 263-3342.
7. Adverse reactions or quality problems experienced with the use of this product
may be reported to the FDA s Med Watch Adverse Event Reporting program
either online, by regular mail or by fax.
Distribution Pattern
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.
Code Information / Serial Numbers
Affected serial numbers for Model # M5066A:
A11K-03264,
A07A-01278,
B07F-01268,
A10G-05443,
A06E-00929,
A06L-01867,
A06L-01678,
A07J-05837,
A10C-03623,
M5066A-ABD,
A07K-02685,
A09H-03908,
0205142344,
Expansion - additional serial numbers for Model # M5066A:
A11K-08837,
Affected Serial numbers for Model # M5067A:
A06K-02421.
Public Record Disclaimer
This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.