Physio-Control, Inc. 2026-05-13 Health serious FDA
Health · FDA · Recall #FDA-Z-2065-2026
LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241,… Recall
Issued May 13, 2026 · Physio-Control, Inc.
In May 2026, Physio-Control, Inc. recalled the LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or inability to provide therapy.
What you should do
- 1 Stop using LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Physio-Control, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Physio-Control, Inc.
- Category
- Health
- Recall date
- May 13, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of MI, WA, KY, IN, FL, NC, TX, LA, VA, NY, MA, CO, PA, OH, SC, OK, MN, WV, NJ, WI.
- Recall number
- FDA-Z-2065-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Physio-Control, Inc. has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.