Safety Alert: Class II: Due to required inspections not being performed on products/units that have gone through servicing.
healthelectronicsClass IIRecalled on Sep 10, 2025
LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-00009
🔢 4 units
Sold At: Physio-Control, Inc.(U.S. Nationwide distribution in the states of CO and MT.)
Recall #: FDA-DEVICE-Z-2497-2025
Source: FDA-ENFORCEMENT
Product Identification
- Lot/Batch Codes:
- Part / Catalog Numbers / UDI-DI code / Serial Number: V15-7-000022 / 99577-001957 / 883873871690 / 49085553 V15-2-000051 / 99577-000046 / 883873988022 / 38154524 V15-2-000099 / 99577-000093 / 883873979020 / 39059475 V15-2-001603 / 99577-001256 / 883873911631 / 40973093
Get AI-Powered Summary
Premium members get instant insights to help you understand recalls faster
Instant 1-3 sentence summary
Quick action bullets
Clear guidance on what to do
Summary
Due to required inspections not being performed on products/units that have gone through servicing.
What to do next
- 1Stop using this product - may cause temporary or medically reversible health problems
- 2Check with retailer or manufacturer for recall status and remedy options
- 3Contact Physio-Control, Inc. for return or refund information
- 4Visit the official FDA recall page for complete details
Summaries only; always follow the official notice.