CLASS II Device recall · Reported 5 Oct 2016 · FDA Enforcement Report
Administration Set, Sterile recalled by Zyno Medical
Zyno Medical is recalling Zyno Medical Administration Set, Sterile, distributed nationwide in the US. The recall was initiated on 29 Jul 2016 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-2893-2016
- FDA event ID
- 74892
- Recalling firm
- Zyno Medical, Natick, MA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 29 Jul 2016
- FDA classified
- 27 Sep 2016
- Reported
- 5 Oct 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Device type
- Heart & Vascular Devices
Timeline
| 29 Jul 2016 | Recall initiated by company | |
| 27 Sep 2016 | Classified by FDA | +60 days |
| 5 Oct 2016 | 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
Administration Set potential filter leaking
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Zyno Medical Administration Set, Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: A2-80071-DF Product Code: A2-80071-DF-120 (Expanded recall) Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a container to a patients vascular system through a needle or a catheter inserted into a vein.
Where it was distributed
US Nationwide Distribution
Questions about this recall
Is Administration Set, Sterile recalled?
Yes. Zyno Medical recalled Administration Set, Sterile on 29 Jul 2016. The recall is Class II and its status is Terminated. Recall number Z-2893-2016.
Why was it recalled?
Administration Set potential filter leaking
Which lots are affected?
Product Code: A2-80071-DF Lot Code: 13125968 13126110 13126111 14026150 14055090 14056598 14065315 14065624 14067149 14075494 14085636 14105960 14106106 14106544 14116251 15045374 15045866 15046986 15055122 15055728 15067196 15085624 15085570 15086315 15086421 15086583 15105241 Product Code:A2-80071-DF-120 Lot code: 15085208
Where was it sold?
US Nationwide Distribution
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 Zyno Medical
All 16| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Z-800F Infusion System recalled by Zyno Medical | Zyno Medical | Device Malfunction | Nationwide |
| Device | CLASS I | Z-800W Infusion System recalled by Zyno Medical | Zyno Medical | Device Malfunction | Nationwide |
| Device | CLASS I | Z-800WF Infusion System recalled by Zyno Medical | Zyno Medical | Device Malfunction | Nationwide |
| Device | CLASS I | Z-800 Infusion System recalled by Zyno Medical | Zyno Medical | Device Malfunction | Nationwide |
| Device | CLASS III | Z-800 Infusion System Z-800WF recalled by Zyno Medical | Zyno Medical | Device Malfunction | 8 states |
Other Heart & Vascular Devices recalls
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|---|---|---|---|---|---|
| Device | CLASS II | Getinge PVC Thoracic Catheter, Soft PVC Right Angle recalled | Atrium Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes: *Bardex¿ I.C recalled | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Getinge PVC Thoracic Catheter, Firm PVC Straight recalled | Atrium Medical | Potency & Assay | Nationwide |