CLASS II Device recall · Reported 19 Aug 2020 · FDA Enforcement Report
STAT KIT Z-1000 emergency medical kit HealthFirst recalled
HF Acquisition is recalling STAT KIT Z-1000 emergency medical kit HealthFirst, distributed nationwide in the US. The recall was initiated on 5 Jun 2020 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2779-2020
- FDA event ID
- 85898
- Recalling firm
- HF Acquisition, Mukilteo, WA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 5 Jun 2020
- FDA classified
- 10 Aug 2020
- Reported
- 19 Aug 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 5 Jun 2020 | Recall initiated by company | |
| 10 Aug 2020 | Classified by FDA | +66 days |
| 19 Aug 2020 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
A missing component (hand suction pump) in the emergency medical kits.
Product as listed by the FDA
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.
Where it was distributed
US Nationwide distribution including in the states of TN and UT.
Questions about this recall
Why was it recalled?
A missing component (hand suction pump) in the emergency medical kits.
Which lots are affected?
STAT KIT Z-1000 Emergency Medical Kit Part Number: 1003550 AMBU Res-Cue Pump part number: 1004330
Where was it sold?
US Nationwide distribution including in the states of TN and UT.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from HF Acquisition
All 10| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Sporetraq Mail-in Spore Testing Service, 12 Tests recalled | HF Acquisition | Device Malfunction | Nationwide |
| Device | CLASS II | Sporetraq Mail-in Spore Testing Service, 52 Tests recalled | HF Acquisition | Device Malfunction | Nationwide |
| Device | CLASS II | Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests recalled | HF Acquisition | Sterility | 50 states |
| Drug | CLASS III | Glycopyrrolate Injection, USP 0.2mg/ML Vial recalledGlycopyrrolate | HF Acquisition | Packaging Defects | AZ, CA, TX |
| Device | CLASS II | HealthFirst Emergency Medical Kit recalled by HF Acquisition Co | HF Acquisition | Packaging Defects | 39 states |
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