EZ Slide Battery/line powered hydraulic table with removable leg… — Class II medical device recall Z-1844-2016
Terminated recall by Skytron, Div. The KMW Group, Inc, reported 2016-06-08, distributed nationwide. The potential exists within the identified tables that incorrectly manufactured parts have been used in assemb
| Recall number | Z-1844-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Skytron, Div. The KMW Group, Inc, Grand Rapids, MI, United States |
| Recall initiated | 2016-04-06 |
| Classified | 2016-05-31 |
| Reported by FDA | 2016-06-08 |
| Terminated | 2017-07-20 |
| Distributed | Nationwide (US) |
| Quantity | 458 |
| Reason classes | device malfunction |
| Model numbers | 3502 |
Product
EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical Table Skytron EZ Slide Operating Table General Purpose Surgical Table
Reason for recall
The potential exists within the identified tables that incorrectly manufactured parts have been used in assembly. If a table is found to have these incorrectly manufactured parts, it is possible for the tables elevation column slide cap to become detached from the elevation column and could result in the loss of control of the table top and injury to the patient or staff.
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-1844-2016. 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.