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FDA Device Recall Monitor

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$10.00 / 1,000 result delivereds

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FDA Device Recall Monitor

FDA Device Recall Monitor

Live openFDA device enforcement and recall rows: firm, product, official link. US FDA only — not a safety certification. $0.02 / row.

Pricing

$10.00 / 1,000 result delivereds

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Developer

Zentra

Zentra

Maintained by Community

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1

Monthly active users

4 days ago

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Power-Trialysis dialysis catheter is a live openFDA row.

Live openFDA device enforcement and recall rows: firm, product, official link. US FDA only — not a safety certification. $0.02 / row.

Last run

10 row(s). First row: **Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; **

{
"title": "Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150;
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; ",
"productName": "Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150;
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; ",
"entityName": "Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150;
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; ",
"listingName": "Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150;
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; ",
"competitorName": "Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150;
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; ",
"buyerName": "OPENFDA-DEVICE-RECALL"
}

Run it

Paste this on the Input tab (JSON) and press Start. That is the same input the last-run used.

{
"buyerQuery": "device recall",
"sourceMode": "startUrls",
"outputMode": "buyer-ready-records",
"maxItems": 10,
"startUrls": [
{
"url": "https://api.fda.gov/device/enforcement.json?limit=10&sort=report_date:desc"
}
]
}

What lands in the dataset

  • openFDA device enforcement
  • Firm, product, official link
  • US only

Use it when

Pull openFDA device enforcement, keep firm + product + official link, and file it next to your CAPA log.

Device QA and competitor-watch teams.

Price

$0.02 / FDA device row — you pay $0.02 per billed result. A 10-row Try is about $0.20.

Schedule it. A one-off curiosity click is not the product.

What you should know

  • Not a safety certification.
  • US FDA only.

FAQ

Is the last-run a fixture? No. The JSON above is from the public source in Run it.

EU MDR certificates? No. US openFDA device enforcement and recalls only.