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Zyno Medical Administration Set, Sterile. Rx recallZ-2893-2016 · Zyno Medical LLC · initiated Jul 29, 2016

Class II Terminated All recalls posted in September 2016

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Zyno Medical LLC or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Administration Set potential filter leaking

FDA root cause category: Process control

What the company is doing

Zyno issued Recall letter dated July 26th, 2016 to affected customers. Customers who received affected products were contacted between 7/29/2016 and 8/1/2016. Customers were asked to return unused product for replacement. For questions contact Customer Service Representative, at 508-907-7796, or [email protected]. Expanded Recall: Two recall letters issued on 11/3/2016 to address the newly identified lots. One letter for customers who received the initial recall letter and the other letter for newly affected customers who did not receive the initial recall letter.

Recall details

Recall number
Z-2893-2016
Recall class
Class II
Status
Terminated
Initiated by the company
Jul 29, 2016
Posted by the FDA
Sep 27, 2016
Recalling firm
Zyno Medical LLC
Quantity
114081 sets
Product code
FPA
FDA submissions
K132841
Distribution
US Nationwide Distribution

Product description

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.

Code information (models, lots, serial numbers)

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

Other devices under the same FDA submission

14 devices cleared under K132841 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 74892).

Sources and updates

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