Physio-Control LIFEPAK CR2 Defibrillator Recall: Required Inspections Not Performed
Physio-Control recalls LIFEPAK CR2 defibrillators due to required inspections not being performed after servicing. Affected units have specific part numbers and serial codes. Consumers should contact the manufacturer for details.
Recall notice
Due to required inspections not being performed on products/units that have gone through servicing.
Contact the company
What happened, in plain English
Physio-Control is recalling LIFEPAK CR2 defibrillators because required inspections weren't done after servicing. This could lead to improper function if the device isn't checked properly after maintenance. Read more at govinfonow.com/recall/51758-physio-control-lifepak-cr2-defibrillator-recall-required-inspections-not-performed.
Source Summary by GovInfoNow · govinfonow.com/recall/51758-physio-control-lifepak-cr2-defibrillator-recall-required-inspections-not-performed · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2499-2025
Cite this page
“Physio-Control LIFEPAK CR2 Defibrillator Recall: Required Inspections Not Performed.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51758-physio-control-lifepak-cr2-defibrillator-recall-required-inspections-not-performed. Based on FDA recall #Z-2499-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2499-2025%22&limit=1).
Why it’s dangerous
The hazard occurs when required inspections after servicing are skipped, which could mean the defibrillator isn't working correctly. This might lead to improper treatment during emergencies if the device fails to function as intended.
Who’s affected
Healthcare professionals who use the LIFEPAK CR2 defibrillator for emergency cardiac care are most at risk. The recall affects specific units with listed part numbers and serial codes.
How to tell if you have this one
Check for part numbers CR2-2-001451, catalog numbers 99512-001434, or UDI-DI code 883873785911 on the device. The recall includes specific units with the serial number 49638156.
- Brand
Physio-Control- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
U.S. Nationwide distribution in the states of CO and MT.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2497-2025 | LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020 V15-2-001603 / 99577-001256 / 883873911631 LIFEPAK 15: The LP15 is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions. The LP15 is designed to be used during ground transportation except when specified otherwise. Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.; 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 | 4 units |
| Z-2498-2025 | LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 331706400001 / 99425-000025 / 885074698953 LIFEPAK 1000: The defibrillator is to be used in AED mode only on patients who are in cardiopulmonary arrest. The patient must be unresponsive, not breathing normally, and showing no signs of circulation. ECG monitoring is for use on conscious and unconscious patients of all ages for the purpose of ECG rhythm recognition and heart rate monitoring.; Part / Catalog Numbers / UDI-DI code / Serial Number: 320371500023 / 99425-000025 / 885074698953 / 35942190 320371500229 / 99425-000025 / 885074698953 / 41012118 331706400001 / 99425-000025 / 885074698953 / 48988273 | 3 units |
| Z-2499-2025 | LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2 defibrillator is indicated for use on patients 1 year of age or older in cardiopulmonary arrest. The patient must be unresponsive (unconscious), not breathing normally, and showing no signs of circulation (for example, no pulse, no coughing, or no movement). The cprCOACHTM Feedback Technology in the LIFEPAK CR2 defibrillator is indicated for use on cardiopulmonary arrest patients and provides CPR guidance in accordance with the AHA Guidelines for patients 1 year of age or older. The LIFEPAK CR2 defibrillator is intended for use by personnel who have been trained in its operation. Users should have received training in basic life support/AED, advanced life support, or a physician-authorized emergency medical response training program.; Part / Catalog Numbers / UDI-DI code / Serial Number: CR2-2-001451 / 99512-001434 / 883873785911 / 49638156 | 1 unit |
What to do — step by step
Check Device Details
Look for part numbers CR2-2-001451, catalog numbers 99512-001434, or UDI-DI code 883873785911 on the device.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 2 states.
FDA distribution: “U.S. Nationwide distribution in the states of CO and MT.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Colorado, Montana.
Recall timeline
FDA published this recall 50 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2499-2025 (July 22, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2499-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.