Physio-Control, Inc. 2023-11-22 Health serious FDA
Health · FDA · Recall #FDA-Z-0296-2024
LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051 Recall
Issued November 22, 2023 · Physio-Control, Inc.
In November 2023, Physio-Control, Inc. recalled the LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
What you should do
- 1 Stop using LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051 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
- November 22, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
- Recall number
- FDA-Z-0296-2024
- 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 903rd Health recall we've logged in 2023.