CLASS II ONGOING Device recall · Reported 9 Oct 2019 · FDA Enforcement Report
Secure Eva - Dual Chamber Container With Screw Connectors, (legless) recalled
The Metrix is recalling Secure Eva - Dual Chamber Container With Screw Connectors, (legless), distributed nationwide in the US. The recall was initiated on 21 Sep 2018 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-0002-2020
- FDA event ID
- 83509
- Recalling firm
- The Metrix, Dubuque, IA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 21 Sep 2018
- FDA classified
- 1 Oct 2019
- Reported
- 9 Oct 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Packaging Defects
- Device type
- Other Medical Devices
Timeline
| 21 Sep 2018 | Recall initiated by company | |
| 1 Oct 2019 | Classified by FDA | +375 days |
| 9 Oct 2019 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential for leaking product
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
Where it was distributed
US Nationwide distribution including the states of PA, MA, IL CA.
Questions about this recall
Is Secure Eva - Dual Chamber Container With Screw Connectors, (legless) recalled?
Yes. The Metrix recalled Secure Eva - Dual Chamber Container With Screw Connectors, (legless) on 21 Sep 2018. The recall is Class II and its status is Ongoing. Recall number Z-0002-2020.
Why was it recalled?
Potential for leaking product
Which lots are affected?
Lot Numbers: 66630-A2771, 66630-A4282
Where was it sold?
US Nationwide distribution including the states of PA, MA, IL CA.
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 21 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 The Metrix
All 33| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Secure Empty Eva Container With 2 Ports recalled by The Metrix | The Metrix | Foreign Material | Nationwide |
| Device | CLASS II | Imed Products Imed EVA, 2-Ports recalled by The Metrix | The Metrix | Foreign Material | Nationwide |
| Device | CLASS II | Secure Empty Eva Container With 2 Ports recalled by The Metrix | The Metrix | Foreign Material | Nationwide |
| Device | CLASS II | Vygon Empty Eva Container With 2 Ports recalled by The Metrix | The Metrix | Foreign Material | Nationwide |
| Device | CLASS II | Secure Empty Eva Container With 2 Ports (Bulk Packed) recalled | The Metrix | Foreign Material | Nationwide |
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| Device | CLASS II | Medline Convenience Kits: Blood Draw Kit recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Ortho Aspiration Kit recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep DYKA1054F recalled | Medline Industries | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Arterial Line Insertion Kit recalled | Medline Industries | Sterility | Nationwide |