RecallRadar

FDA Device recall Z-2893-2016

Zyno Medical Administration Set, Sterile

On 2016-10-05 the FDA classified a Class II recall of Zyno Medical Administration Set, Sterile by Zyno Medical, citing administration Set potential filter leaking.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2893-2016
ClassificationClass II
Statusterminated
Initiated2016-07-29
Published2016-10-05
Last updated2026-09-13 11:54 UTC
CompanyZyno Medical
DistributionUS

Product

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.

Reason

Administration Set potential filter leaking

Identifiers

code_info
Product Code: A2-80071-DF Lot Code: 13125968 13126110 13126111 14026150 14055090 14056598 14065315 14065624 1…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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2893-2016%22

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