T100-120F with 1 — Class II medical device recall Z-2233-2016
Terminated recall by WalkMed Infusion, LLC, reported 2016-07-27, distributed nationwide. WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton Administration Sets Due to the Pot
| Recall number | Z-2233-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | WalkMed Infusion, LLC, Englewood, CO, United States |
| Recall initiated | 2016-06-14 |
| Classified | 2016-07-18 |
| Reported by FDA | 2016-07-27 |
| Terminated | 2016-12-01 |
| Distributed | Nationwide (US) |
| Quantity | 295 cases |
| Reason classes | specification failure |
| Lot numbers | 1412070D, 1502055D, 1503039D, 1505047D, 1506051D, 1506052D |
Product
T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
Reason for recall
WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton Administration Sets Due to the Potential Presence of Particulate In or On the Administration Sets.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2233-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.