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Med Halowerk Device Recall Search
x402
Med Halowerk Device Recall Search is a paid API for AI agents from med.halowerk.com, paid per call via x402, $0.005/call, status unknown (last checked 2026-10-13).
Searches the FDA medical device recall database by product name, manufacturer, or model and returns matching recalls with classification, reason, recalling firm, dates, status, and verbatim product descriptions including lot numbers and serial ranges.
Price / call$0.005
Success—
StatusUnknown
How this service works
Searches the device recall database for a product, manufacturer or model and returns each matching recall with the classification and its meaning, the reason, the recalling firm, the dates, the status and — the field that decides whether a specific unit is affected — the product description including lot numbers and serial ranges, quoted verbatim.
Output
Returns an array of matching recall records, each containing: recall classification (Class I, II, or III) and its meaning, the reason for the recall, the recalling firm name, initiation and termination dates, current recall status, and the verbatim product description including specific lot numbers and serial number ranges needed to determine whether a particular unit is affected.
Example use cases
Checking a specific device unit's recall status
“I have a Philips Respironics DreamStation CPAP with serial number C17212075XXXXX — can you check if there's a recall covering that unit and what the recall reason and classification are?”
Hospital procurement safety screening
“We're considering purchasing cardiac defibrillators from Zoll Medical — can you pull any recalls on their devices, including the classification level, what was wrong, and what product lots are involved?”
Patient safety notification workflow
“My doctor's office uses Abbott FreeStyle Libre readers and wants to know if any models have been recalled by the FDA, including the full product description with affected lot numbers and the current recall status.”
Technical details
Endpoint
POSThttps://med.halowerk.com/v1/device-recall?utm_source=zero.xyzWhen to prefer
Use this endpoint when you need to determine whether a specific medical device, identified by product name, manufacturer, or model, is subject to an FDA recall — especially when you need to verify whether a particular unit (by lot number or serial range) is affected. Prefer this over general web search when you need structured, authoritative FDA recall data with classification severity and verbatim product scope descriptions. Choose this over the drug recall sibling endpoint when the subject is a device (not a pharmaceutical).
Side effects
- No matches found for the given product, manufacturer, or model — returns empty results
- Ambiguous search term matches too many or unrelated products — requires more specific input
- FDA database unavailable or rate-limited — service returns error
- Product exists but has no recall history — empty result set that may be mistaken for a lookup failure
- Lot numbers or serial ranges not available for older recalls — product description field may be incomplete
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| limit | integer | |
| since | string | ISO date; defaults to three years back. |
| device | string | Device name or model. |
| manufacturer | string |
Tags
x402
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