RecallRadar

FDA Device recall Z-2895-2016

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-2895-2016
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: B2-70071-DF Product Code: B2-70071-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
B2-70071-DF Lot Codes: 14015279 14026620 14046841 14055191 14055786 14056225 14085743 14085742 15035297 15045…B2-70071-DF Lot Codes: 14015279 14026620 14046841 14055191 14055786 14056225 14085743 14085742 15035297 15045941 15045940 15046600 15075275 15075835 15076761 15085107 15086621 15095200 15095647 15097179 15105595 B2-70071-DF-120 lot codes: 15066912 15075253 15075990 15076261 15076304

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-2895-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.