Which device
The model and serial number from the DME delivery ticket, the recall registration and the replacement record, side by side.
serial on fileNewMissing Records Detection: flags every visit, provider, and date missing from the file. See how →
- Solutions
- Case types
- Philips CPAP
The recall names the device. The case has to name the serial number.
Medrecords AI lines up the device file with the medical file: the DME delivery, the serial number, the usage downloads, the recall and the replacement, then the symptoms, the diagnosis and every other cause the chart records. Every entry links to its page.
- HIPAA, under a BAA
- SOC 2
- 100 pages a minute
- First case is free on us
1 device, 2 filestap a point
Device file
Medical file
15 Feb 2022Replacement recordDevice file
Replacement device shipped. Original returned.
Illustrative case. The patient, device, dates and pages are fictional. The recall date is real.
15Mdevices
Roughly how many Philips sleep and breathing devices the June 2021 recall covered worldwide.
Philips$1.075Bsettlement
The personal injury settlement Philips agreed to in 2024.
Philips, MDL No. 30143014MDL
The federal CPAP litigation, centralized in the Western District of Pennsylvania.
JPML, MDL No. 3014100pages a minute
How fast Medrecords AI reads the file.
Medrecords AI
Where CPAP cases turn
Device file Device file Device file Medical file Medical file Both
6 places the claims review looks first. The chronology gets you there before it does.
A CPAP claim needs the right device, enough use and a diagnosis on the list. These are the points where it gets decided, each flagged with its page.
How much use
Usage downloads and compliance reports in order, so hours of use have pages behind them.
use patternThe recall and the replacement
When the device was registered, replaced and returned. A returned device changes what can be tested.
device returnedSymptom onset
The first note of cough, sinus problems or breathing trouble, dated and quoted, set against the years of use.
symptom onsetEvery other cause
Smoking, work exposures, family history and prior lung disease the chart records, each with its page.
other cause notedThe records that never arrived
The DME ticket, the usage download, the pathology report a note mentions. Listed with the page that points to each one.
missing-records list
Sample output
What comes back: the device file and the medical file, every line cited.
| Date | Source | Finding | Page | Flag |
|---|---|---|---|---|
| 12 Apr 2017 | DME delivery ticket | DreamStation delivered. Serial number on the ticket. | p. 3 | serial on file |
| 1 Oct 2019 | Usage download | Used on 94% of nights, 7 hours on average. | p. 8 | use pattern |
| 1 Jul 2021 | Recall registration | Serial registered on the recall site. | p. 11 | cited |
| 15 Feb 2022 | Replacement record | Replacement device shipped. Original returned. | p. 14 | device returned |
| Date | Source | Finding | Page | Flag |
|---|---|---|---|---|
| 9 Sep 2012 | Primary care | Former smoker, 15 pack-years. | p. 18 | other cause noted |
| 3 Mar 2017 | Sleep study | Moderate obstructive sleep apnea. CPAP prescribed. | p. 20 | cited |
| 10 Jun 2020 | Pulmonology | Chronic cough and sinus irritation. | p. 31 | symptom onset |
| 22 Nov 2022 | CT chest | Spiculated nodule, right upper lobe. | p. 44 | cited |
| 5 Jan 2023 | Pathology | Biopsy: lung adenocarcinoma. | p. 52 | cited |
Fictional case built for this page. Real output carries the same columns, with every page linked to the source PDF.
How it works
Send both files. Get 1 timeline back.
What you send
- DME delivery tickets, usage downloads and recall records
- Sleep study, pulmonology and oncology records
- Imaging and pathology reports
- Pharmacy and primary care records
- Any format: PDFs, scans, faxes, phone photos
What you get
- Device model and serial number, with pages
- Usage over time from every download in the file
- Symptom onset and diagnosis in order
- Every alternative cause the chart records
- A list of records the file refers to but does not contain
We lay out the record. Your experts give the causation opinion.
We assemble and cite the device history, the use and the medical course. We do not say the foam caused the illness, decide settlement eligibility or value the claim. Those belong to your experts and the claims process.
HIPAA, under a signed BAAEvery file is handled under our Business Associate Agreement.
SOC 2Encryption in transit and at rest, and PHI access logging on every event.
Never trains a modelYour records never train any AI model, ours or anyone else’s.
Deleted after deliveryFiles are deleted 30 days after delivery, with an audit log of every access.
Questions
Philips CPAP case review, answered.
Can you confirm the device was part of the recall?
We pull the model and serial number from every record that shows them, with pages. Whether that device was covered is checked against the recall list by you.
Can you read usage downloads?
Yes, if you have them as documents or printouts. Compliance reports and usage summaries are read like any other record and placed on the timeline.
Does this help with settlement claim packets?
Yes. The device, use, diagnosis and dates are pulled into 1 cited summary per claimant, ready for your team to check against the claim criteria.
Do you retrieve records from providers?
No. Medrecords AI does not retrieve records from providers or facilities. You bring the records you already have, and review starts in minutes from upload.
Related case types
Send us 1 CPAP case. The first case is free on us.
Book a short demo. After it we open trial access on one of your own cases, the first one free on us, with the chronology back page-cited.