Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported November 28, 2012
RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention of pulmonary complications as a result of immobility, Thoracic or lumbar fracture, Cervical traction, Skeletal traction
The firm is initiating a voluntary medical device correction for the RotoRest Delta Therapy System head pack. KCI has received complaints alleging patients experiencing skin brea…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Kci USA, Inc. recalled RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention of pulmona… - a moderate-severity action.
RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention of pulmona… was recalled by Kci USA, Inc. in November 28, 2012. Reason: The firm is initiating a voluntary medical device correction for the RotoRest Delta Therapy System head pack.…. Check the official notice for the remedy. Verify recall #Z-0409-2013 with the FDA Devices before acting.
The recall
Kci USA, Inc. issued this moderate-severity FDA Devices recall-The firm is initiating a voluntary medical device correction for the RotoRest Delta Therapy System head pack.….
- Moderate
- severity level
- 282 units
- affected scope
- Class II
- classification
- November 28, 2012
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0409-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0409-2013) was formally reported on November 28, 2012, with the manufacturer initiating the action on June 27, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Kci USA, Inc. is listed as the recalling firm, operating out of San Antonio, TX. Federal records list the affected scope as 282 units.
The documented reason for this recall is: The firm is initiating a voluntary medical device correction for the RotoRest Delta Therapy System head pack. KCI has received complaints alleging patients experiencing skin breakdown on the head and face due to the po… Distribution data in the federal record shows the product reached: Nationwide Distribution including AL, CA, CO, OK and GA.. 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
282 units
Related Recalls
6
3 from same agency
Product description
RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention of pulmonary complications as a result of immobility, Thoracic or lumbar fracture, Cervical traction, Skeletal traction
Reason for recall
The firm is initiating a voluntary medical device correction for the RotoRest Delta Therapy System head pack. KCI has received complaints alleging patients experiencing skin breakdown on the head and face due to the positioning of the head pack. In a few instances, the patient received injuries ranging from Stage III to Stage IV pressure ulcers.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0409-2013 |
| Date reported | November 28, 2012 |
| Date initiated | June 27, 2012 |
| Recalling firm | Kci USA, Inc. |
| Firm location | San Antonio, TX |
| Affected scope | 282 units |
| Distribution | Nationwide Distribution including AL, CA, CO, OK and GA. |
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-0409-2013) 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? ▼
RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention of pulmonary complications as a result of immobility, Thoracic or lumbar fracture, Cervical traction, Skeletal traction. Recalled by Kci USA, Inc.. Units affected: 282 units.
Why was this product recalled? ▼
The firm is initiating a voluntary medical device correction for the RotoRest Delta Therapy System head pack. KCI has received complaints alleging patients experiencing skin breakdown on the head and face due to the positioning of the head pack. In a few instances, the patient received injuries ranging from Stage III to Stage IV pressure ulcers.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 28, 2012. Severity: Moderate. Recall number: Z-0409-2013.
Where was the recalled product distributed? ▼
Distribution: Nationwide Distribution including AL, CA, CO, OK and GA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0409-2013) 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 November 28, 2012. 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.