LIFEPAK 35 ECG cable REF 11111-000041
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog Number: 11111-000041 UDI-DI code: 00883873834596 Lot/Serial Number: 0224
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Physio-Control, Inc.
- Reason for Recall:
- Product shipped with incorrect IFU. IFU does not include proper cleaning/disinfection instructions
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
LIFEPAK 35 ECG cable REF 11111-000041
Product Codes/Lot Numbers:
Catalog Number: 11111-000041 UDI-DI code: 00883873834596 Lot/Serial Number: 0224
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1102-2025
Related Recalls
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.
Due to pediatric defibrillator electrode delamination
Due to required inspections not being performed on products/units that have gone through servicing.