← The evidence ledger
Evidence row 77205
Observed , by baseline/1.
- Kind
- listing
- About
- source_record x402_bazaar:https://loonie-toll.onrender.com/device
- Recorded
- Previous row
- None: the first of its kind about this subject
- Body SHA-256
- 815d4e7ec61beed01a26e36830c199173338aa27a701772a37abba78802dc560
- Leaf
- 0xb2bc32100d69c228dc700a2ab455c92134b21d89500e12378954154455fbfa71
What was observed
{
"endpoints": [
[
"x402",
"https://loonie-toll.onrender.com/device"
]
],
"name": "ClearCheck",
"owner_address": "0xb531320805c5bed1d46aeadcf4f008fdf172dbda",
"raw": {
"accepts": [
{
"amount": "30000",
"asset": "0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913",
"extra": {
"name": "USD Coin",
"version": "2"
},
"maxTimeoutSeconds": 300,
"network": "eip155:8453",
"payTo": "0xb531320805C5BED1D46AEaDcF4F008FDF172DBDa",
"scheme": "exact"
},
{
"amount": "30000",
"asset": "EPjFWdd5AufqSSqeM2qN1xzybapC8G4wEGGkZwyTDt1v",
"extra": {
"feePayer": "BENrLoUbndxoNMUS5JXApGMtNykLjFXXixMtpDwDR9SP"
},
"maxTimeoutSeconds": 300,
"network": "solana:5eykt4UsFv8P8NJdTREpY1vzqKqZKvdp",
"payTo": "DUPiupXtuox38dcGoXUKer5mAydCzmaHjrbQ66qeEm8s",
"scheme": "exact"
},
{
"amount": "30000",
"asset": "0x3c499c542cEF5E3811e1192ce70d8cC03d5c3359",
"extra": {
"name": "USD Coin",
"version": "2"
},
"maxTimeoutSeconds": 300,
"network": "eip155:137",
"payTo": "0xb531320805C5BED1D46AEaDcF4F008FDF172DBDa",
"scheme": "exact"
},
{
"amount": "30000",
"asset": "0xaf88d065e77c8cC2239327C5EDb3A432268e5831",
"extra": {
"name": "USD Coin",
"version": "2"
},
"maxTimeoutSeconds": 300,
"network": "eip155:42161",
"payTo": "0xb531320805C5BED1D46AEaDcF4F008FDF172DBDa",
"scheme": "exact"
}
],
"description": "Is this medical device FDA-cleared, and has it been recalled? 510(k) clearances joined to recall enforcement.",
"extensions": {
"bazaar": {
"info": {
"input": {
"method": "GET",
"queryParams": {
"firm": "Medtronic"
},
"type": "http"
},
"output": {
"example": {
"clearances": [
{
"advisoryPanel": "Neurology",
"applicant": "Medtronic Xomed, Inc.",
"clearanceType": "Traditional",
"decidedOn": "2026-09-04",
"decision": "Substantially Equivalent",
"deviceName": "ApexCut Blade with Automated EM Tracking (187BL4012EM);ApexCut Blade with Automated EM Tracking (187BL4040EM);ApexCut Blade with Automated EM Tracking (187BL4060EM);ApexCut Blade with Automate…",
"kNumber": "K262235",
"location": "Jacksonville, FL, US",
"productCode": "PGW",
"receivedOn": "2026-07-01"
},
{
"advisoryPanel": "Cardiovascular",
"applicant": "Medtronic, Inc.",
"clearanceType": "Special",
"decidedOn": "2026-08-28",
"decision": "Substantially Equivalent",
"deviceName": "LINQ II Insertable Cardiac Monitor (ICM) (LNQ22)",
"kNumber": "K262735",
"location": "Mounds View, MN, US",
"productCode": "MXD",
"receivedOn": "2026-07-31"
}
],
"counts": {
"clearances": 1586,
"openRecalls": 8,
"recalls": 1917
},
"disclaimer": "Advisory only, provided as is without warranty of accuracy or completeness. Absence of a 510(k) record is not proof a device is uncleared — exempt and PMA-approved devices are not in this dataset. Not…",
"query": {
"device": null,
"firm": "Medtronic"
},
"reasons": [
"1586 510(k) clearance(s) on record, but 8 recall(s) are still open.",
"Most recent open recall: Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture i"
],
"recalls": [
{
"action": "On 7/13/2026, field safety notices were sent to customers asking them to do the following:\n1) Stop using the loaner pump and contact the firm to arrange for loaner pump return. \n2) Contact your Health…",
"distribution": "International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.",
"initiatedOn": "2026-07-13",
"postedOn": "2026-08-18",
"product": "MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;",
"quantity": "16",
"reason": "Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, poten…",
"recallNumber": "Z-2980-2026",
"recallingFirm": "Medtronic MiniMed, Inc.",
"relatedClearances": [
"K251032"
],
"rootCause": "Process design",
"status": "Open, Classified",
"terminatedOn": null
},
{
"action": "On 7/13/2026, field safety notices were sent to customers asking them to do the following:\n1) Stop using the loaner pump and contact the firm to arrange for loaner pump return. \n2) Contact your Health…",
"distribution": "International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.",
"initiatedOn": "2026-07-13",
"postedOn": "2026-08-18",
"product": "MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;",
"quantity": "7",
"reason": "Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, poten…",
"recallNumber": "Z-2981-2026",
"recallingFirm": "Medtronic MiniMed, Inc.",
"relatedClearances": [],
"rootCause": "Process design",
"status": "Open, Classified",
"terminatedOn": null
}
],
"retrievedAt": "2026-09-17T16:24:10.414Z",
"source": "openFDA — 510(k) clearances and device recall enforcement (US FDA)",
"verdict": "CLEARED_WITH_OPEN_RECALL"
},
"type": "json"
}
},
"schema": {
"$schema": "https://json-schema.org/draft/2020-12/schema",
"properties": {
"input": {
"additionalProperties": false,
"properties": {
"method": {
"enum": [
"GET"
],
"type": "string"
},
"queryParams": {
"properties": {
"device": {
"description": "Device name or type, e.g. 'infusion pump'",
"type": "string"
},
"firm": {
"description": "Manufacturer or applicant name",
"type": "string"
},
"limit": {
"description": "Max records per section, default 8",
"type": "integer"
}
},
"required": [],
"type": "object"
},
"type": {
"const": "http",
"type": "string"
}
},
"required": [
"type",
"method"
],
"type": "object"
},
"output": {
"properties": {
"example": {
"properties": {
"clearances": {
"items": {
"properties": {
"advisoryPanel": {
"type": [
"null",
"string"
]
},
"applicant": {
"type": [
"null",
"string"
]
},
"clearanceType": {
"type": [
"null",
"string"
]
},
"decidedOn": {
"type": [
"null",
"string"
]
},
"decision": {
"type": [
"null",
"string"
]
},
"deviceName": {
"type": [
"null",
"string"
]
},
"kNumber": {
"type": [
"null",
"string"
]
},
"location": {
"type": [
"null",
"string"
]
},
"productCode": {
"type": [
"null",
"string"
]
},
"receivedOn": {
"type": [
"null",
"string"
]
}
},
"type": "object"
},
"type": [
"array",
"null"
]
},
"counts": {
"properties": {
"clearances": {
"type": [
"null",
"number"
]
},
"openRecalls": {
"type": [
"null",
"number"
]
},
"recalls": {
"type": [
"null",
"number"
]
},
"recallsChecked": {
"type": "boolean"
}
},
"type": [
"null",
"object"
]
},
"disclaimer": {
"type": [
"null",
"string"
]
},
"query": {
"properties": {
"device": {},
"firm": {
"type": [
"null",
"string"
]
}
},
"type": [
"null",
"object"
]
},
"reasons": {
"items": {
"type": "string"
},
"type": [
"array",
"null"
]
},
"recalls": {
"items": {
"properties": {
"action": {
"type": [
"null",
"string"
]
},
"distribution": {
"type": [
"null",
"string"
]
},
"initiatedOn": {
"type": [
"null",
"string"
]
},
"postedOn": {
"type": [
"null",
"string"
]
},
"product": {
"type": [
"null",
"string"
]
},
"quantity": {
"type": [
"null",
"string"
]
},
"reason": {
"type": [
"null",
"string"
]
},
"recallNumber": {
"type": [
"null",
"string"
]
},
"recallingFirm": {
"type": [
"null",
"string"
]
},
"relatedClearances": {
"items": {
"type": "string"
},
"type": [
"array",
"null"
]
},
"rootCause": {
"type": [
"null",
"string"
]
},
"status": {
"type": [
"null",
"string"
]
},
"terminatedOn": {}
},
"type": "object"
},
"type": [
"array",
"null"
]
},
"retrievedAt": {
"type": [
"null",
"string"
]
},
"source": {
"type": [
"null",
"string"
]
},
"verdict": {
"type": [
"null",
"string"
]
}
},
"type": "object"
},
"type": {
"type": "string"
}
},
"required": [
"type"
],
"type": "object"
}
},
"required": [
"input"
],
"type": "object"
}
}
},
"lastUpdated": "2026-10-20T20:53:17.241Z",
"quality": {
"l30DaysTotalCalls": 2,
"l30DaysUniquePayers": 2,
"lastCalledAt": "2026-10-20T20:53:16.839Z"
},
"resource": "https://loonie-toll.onrender.com/device",
"serviceName": "ClearCheck",
"tags": [
"government-data",
"compliance",
"verification",
"public-records",
"risk-screening"
],
"type": "http",
"x402Version": 2
},
"source": "x402_bazaar",
"summary": "Is this medical device FDA-cleared, and has it been recalled? 510(k) clearances joined to recall enforcement."
}What the leaf hashes
{"body":"815d4e7ec61beed01a26e36830c199173338aa27a701772a37abba78802dc560","id":77205,"kind":"listing","method":"baseline/1","observed_us":1793025493459764,"prev":null,"subject":"x402_bazaar:https://loonie-toll.onrender.com/device","subject_kind":"source_record"}Proof
Its day has not closed yet. A day closes ten minutes after midnight UTC; the proof appears here then.