STAT KIT Z-1000 emergency medical kit HealthFirst — Class II medical device recall Z-2779-2020
Terminated recall by HF Acquisition Co. LLC, reported 2020-08-19, distributed nationwide. A missing component (hand suction pump) in the emergency medical kits.
| Recall number | Z-2779-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | HF Acquisition Co. LLC, Mukilteo, WA, United States |
| Recall initiated | 2020-06-05 |
| Classified | 2020-08-10 |
| Reported by FDA | 2020-08-19 |
| Terminated | 2022-02-01 |
| Distributed | Nationwide (US) |
| Quantity | 2 kits |
| Model numbers | 1003550, 1004330 |
Product
STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced cardiac life support devices and medications to respond to cardiopulmonary medical emergencies until EMS arrives.
Reason for recall
A missing component (hand suction pump) in the emergency medical kits.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2779-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.