Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported June 8, 2016
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
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,…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Skytron, Div. The Kmw Group, Inc recalled EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slid… - a moderate-severity action.
EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slid… was recalled by Skytron, Div. The Kmw Group, Inc in June 8, 2016. Reason: The potential exists within the identified tables that incorrectly manufactured parts have been used in assem…. Check the official notice for the remedy. Verify recall #Z-1844-2016 with the FDA Devices before acting.
The recall
Skytron, Div. The Kmw Group, Inc issued this moderate-severity FDA Devices recall-The potential exists within the identified tables that incorrectly manufactured parts have been used in assem….
- Moderate
- severity level
- 458 units
- affected scope
- Class II
- classification
- June 8, 2016
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1844-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1844-2016) was formally reported on June 8, 2016, with the manufacturer initiating the action on April 6, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Skytron, Div. The Kmw Group, Inc is listed as the recalling firm, operating out of Grand Rapids, MI. Federal records list the affected scope as 458.
The documented reason for this recall is: 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 elevatio… Distribution data in the federal record shows the product reached: Nationwide Distribution to AL, AZ, CO, IA, WI, PA, TN, MA, TX, MI, FL, MS, LA, and CA.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
458
Related Recalls
6
3 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1844-2016 |
| Date reported | June 8, 2016 |
| Date initiated | April 6, 2016 |
| Recalling firm | Skytron, Div. The Kmw Group, Inc |
| Firm location | Grand Rapids, MI |
| Affected scope | 458 |
| Distribution | Nationwide Distribution to AL, AZ, CO, IA, WI, PA, TN, MA, TX, MI, FL, MS, LA, and CA. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1844-2016) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Skytron, Div. The Kmw Group, Inc. Units affected: 458.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 8, 2016. Severity: Moderate. Recall number: Z-1844-2016.
Where was the recalled product distributed? ▼
Distribution: Nationwide Distribution to AL, AZ, CO, IA, WI, PA, TN, MA, TX, MI, FL, MS, LA, and CA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1844-2016) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported June 8, 2016. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.