The EKOS cart has the catalog number 700-60101 — Class II medical device recall Z-2890-2016
Terminated recall by EKOS Corporation, reported 2016-10-05, distributed nationwide. Casters on the EKOS carts may be missing washers which can cause premature wear and dislodgement of the caster
| Recall number | Z-2890-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | EKOS Corporation, Bothell, WA, United States |
| Recall initiated | 2016-08-22 |
| Classified | 2016-09-27 |
| Reported by FDA | 2016-10-05 |
| Terminated | 2016-12-30 |
| Distributed | Nationwide (US) |
| Quantity | 455 units |
| Lot numbers | 010416, 011816, 022216, 030915, 032116, 032615, 040915, 052416, 061515, 071515, 081715, 103015, 120715 |
| Model numbers | 700-60101 |
Product
The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and transport the EkoSonic Control Unit. The cart is designed with three poles to hold infusion pumps and fluid bags, a tray on which the EkoSonic Control unit sits and a base designed to hold an Uninterruptable Power Supply (UPS). The cart mounts on 4 wheels, two locking and two non-locking.
Reason for recall
Casters on the EKOS carts may be missing washers which can cause premature wear and dislodgement of the casters/wheels leading to failure.
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-2890-2016. 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.