{
    "status": "real_sample_available",
    "actor_slug": "fda-safety-signal-monitor-v2",
    "family": "recall_compliance",
    "family_label": "Recall, safety, and compliance actor",
    "generated_at": "2026-07-26T16:05:01.782659Z",
    "source_provenance": {
        "kind": "stored_actor_quality_run",
        "apify_run_id": "",
        "default_dataset_id": "",
        "finished_at": "2026-07-23T11:56:17.000000Z"
    },
    "items": [
        {
            "score": 92,
            "errors": [],
            "status": "Open, Classified",
            "summary": "Labeling discrepancy:  Devices distributed with Instructions For Use (IFU) did not include\r\nFARAPOINT PFA catheter information.",
            "recordId": "fda-safety-signal-monitor-v2:OPENFDA-DEVICE-RECALL:Z-2750-2026",
            "dedupeKey": "fda-safety-signal-monitor-v2:OPENFDA-DEVICE-RECALL:Z-2750-2026",
            "sourceUrl": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=221107",
            "confidence": 0.9,
            "entityName": "FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter",
            "entityType": "medical_device",
            "runSummary": {
                "mode": "startUrls",
                "recordsSaved": 1,
                "sinceLastRun": true,
                "watchlistTerms": [],
                "sourceDiscovery": "openfda-device-recall-api"
            },
            "signalType": "device_recall",
            "sourceName": "OPENFDA-DEVICE-RECALL",
            "effectiveAt": "2026-07-17",
            "retrievedAt": "2026-07-23T11:56:16.880Z",
            "jurisdiction": "US",
            "scoreReasons": [
                "openFDA device recall API result",
                "Matched openFDA device recall API record.",
                "openFDA records are unvalidated and do not prove causation or replace medical advice."
            ],
            "recordIdentifier": "Z-2750-2026",
            "recommendedAction": "Boston Scientific issued an Urgent Field Safety Notice - Urgent Medical Device Correction notice to its consignees out side the US on 6/11/2026 via hand delivered letter.  The notice explained the issue and requested the following actions be taken:  \nInstructions:  \n1- Post a copy of the appropriate IFU provided near each FARASTAR PFA generator, replacing any previous versions currently in use.  \n2- Review the IFU and ensure all relevant personnel are aware of its contents.  \n3- Please complete the attached Acknowledgement Form even if you do not have any affected product and return it to your Boston Scientific office.\n4- Share this communication with any healthcare professionals in your facility that use the product and with any other organization to which this product may have been transferred. \nThe national Competent Authority was informed of this communication. Any adverse events or quality concerns associated with use of these devices should be reported to Boston Scientific and Competent Authorities if appropriate."
        },
        {
            "score": 92,
            "errors": [],
            "status": "Open, Classified",
            "summary": "Labeling discrepancy:  Devices distributed with Instructions For Use (IFU) did not include\r\nFARAPOINT PFA catheter information.",
            "recordId": "fda-safety-signal-monitor-v2:OPENFDA-DEVICE-RECALL:Z-2751-2026",
            "dedupeKey": "fda-safety-signal-monitor-v2:OPENFDA-DEVICE-RECALL:Z-2751-2026",
            "sourceUrl": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=221111",
            "confidence": 0.9,
            "entityName": "FARASTAR Pulsed Field Ablation Generator, Product ID M004PFCE61M401; Percutaneous Cardiac Ablation Catheter",
            "entityType": "medical_device",
            "runSummary": {
                "mode": "startUrls",
                "recordsSaved": 2,
                "sinceLastRun": true,
                "watchlistTerms": [],
                "sourceDiscovery": "openfda-device-recall-api"
            },
            "signalType": "device_recall",
            "sourceName": "OPENFDA-DEVICE-RECALL",
            "effectiveAt": "2026-07-17",
            "retrievedAt": "2026-07-23T11:56:16.977Z",
            "jurisdiction": "US",
            "scoreReasons": [
                "openFDA device recall API result",
                "Matched openFDA device recall API record.",
                "openFDA records are unvalidated and do not prove causation or replace medical advice."
            ],
            "recordIdentifier": "Z-2751-2026",
            "recommendedAction": "Boston Scientific issued an Urgent Field Safety Notice - Urgent Medical Device Correction notice to its consignees out side the US on 6/11/2026 via hand delivered letter.  The notice explained the issue and requested the following actions be taken:  \nInstructions:  \n1- Post a copy of the appropriate IFU provided near each FARASTAR PFA generator, replacing any previous versions currently in use.  \n2- Review the IFU and ensure all relevant personnel are aware of its contents.  \n3- Please complete the attached Acknowledgement Form even if you do not have any affected product and return it to your Boston Scientific office.\n4- Share this communication with any healthcare professionals in your facility that use the product and with any other organization to which this product may have been transferred. \nThe national Competent Authority was informed of this communication. Any adverse events or quality concerns associated with use of these devices should be reported to Boston Scientific and Competent Authorities if appropriate."
        },
        {
            "score": 92,
            "errors": [],
            "status": "Open, Classified",
            "summary": "Labeling discrepancy:  Devices distributed with Instructions For Use (IFU) did not include\r\nFARAPOINT PFA catheter information.",
            "recordId": "fda-safety-signal-monitor-v2:OPENFDA-DEVICE-RECALL:Z-2752-2026",
            "dedupeKey": "fda-safety-signal-monitor-v2:OPENFDA-DEVICE-RECALL:Z-2752-2026",
            "sourceUrl": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=221113",
            "confidence": 0.9,
            "entityName": "FARASTAR PFA Generator, Product ID M004PFCE61M460; Percutaneous Cardiac Ablation Catheter",
            "entityType": "medical_device",
            "runSummary": {
                "mode": "startUrls",
                "recordsSaved": 3,
                "sinceLastRun": true,
                "watchlistTerms": [],
                "sourceDiscovery": "openfda-device-recall-api"
            },
            "signalType": "device_recall",
            "sourceName": "OPENFDA-DEVICE-RECALL",
            "effectiveAt": "2026-07-17",
            "retrievedAt": "2026-07-23T11:56:17.034Z",
            "jurisdiction": "US",
            "scoreReasons": [
                "openFDA device recall API result",
                "Matched openFDA device recall API record.",
                "openFDA records are unvalidated and do not prove causation or replace medical advice."
            ],
            "recordIdentifier": "Z-2752-2026",
            "recommendedAction": "Boston Scientific issued an Urgent Field Safety Notice - Urgent Medical Device Correction notice to its consignees out side the US on 6/11/2026 via hand delivered letter.  The notice explained the issue and requested the following actions be taken:  \nInstructions:  \n1- Post a copy of the appropriate IFU provided near each FARASTAR PFA generator, replacing any previous versions currently in use.  \n2- Review the IFU and ensure all relevant personnel are aware of its contents.  \n3- Please complete the attached Acknowledgement Form even if you do not have any affected product and return it to your Boston Scientific office.\n4- Share this communication with any healthcare professionals in your facility that use the product and with any other organization to which this product may have been transferred. \nThe national Competent Authority was informed of this communication. Any adverse events or quality concerns associated with use of these devices should be reported to Boston Scientific and Competent Authorities if appropriate."
        }
    ]
}