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 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 3317064000
🔢 3 units
Sold At: Physio-Control, Inc.(U.S. Nationwide distribution in the states of CO and MT.)
Recall #: FDA-DEVICE-Z-2498-2025
Source: FDA-ENFORCEMENT
Product Identification
- Lot/Batch Codes:
- Part / Catalog Numbers / UDI-DI code / Serial Number: 320371500023 / 99425-000025 / 885074698953 / 35942190 320371500229 / 99425-000025 / 885074698953 / 41012118 331706400001 / 99425-000025 / 885074698953 / 48988273
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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.