Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported February 12, 2014
The Rotoprone therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications. The Rotoprone Therapy System provides up to 62 degrees in both prone and supine positions as well as Trendelenburg/Reverse Trendelenburg positioning. Product Usage: Use of the Rotoprone Therapy System is indicated for patients with severe acute respiratory distress syndrome (ARDS). These are critical patients who are at higher risk of cardiac arrest and mortality. Pl
The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to prone a patient
ArjoHuntleigh Inc. recalled The Rotoprone therapy System is an advanced patient care system for the treatment and pre… - a moderate-severity action.
The Rotoprone therapy System is an advanced patient care system for the treatment and pre… was recalled by ArjoHuntleigh Inc. in February 12, 2014. Reason: The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to …. Check the official notice for the remedy. Verify recall #Z-0926-2014 with the FDA Devices before acting.
The recall
ArjoHuntleigh Inc. issued this moderate-severity FDA Devices recall-The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to ….
- Moderate
- severity level
- 231 units
- affected scope
- Class II
- classification
- February 12, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0926-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0926-2014) was formally reported on February 12, 2014, with the manufacturer initiating the action on September 11, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. ArjoHuntleigh Inc. is listed as the recalling firm, operating out of San Antonio, TX. Federal records list the affected scope as 231 units.
The documented reason for this recall is: The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to prone a patient Distribution data in the federal record shows the product reached: US Nationwide and Middle East. 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
231 units
Related Recalls
6
3 from same agency
Product description
The Rotoprone therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications. The Rotoprone Therapy System provides up to 62 degrees in both prone and supine positions as well as Trendelenburg/Reverse Trendelenburg positioning. Product Usage: Use of the Rotoprone Therapy System is indicated for patients with severe acute respiratory distress syndrome (ARDS). These are critical patients who are at higher risk of cardiac arrest and mortality. Placing a patient in the prone position may reopen collapsed airways and thus improve pulmonary gas exchange and respiratory mechanics.
Reason for recall
The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to prone a patient
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0926-2014 |
| Date reported | February 12, 2014 |
| Date initiated | September 11, 2013 |
| Recalling firm | ArjoHuntleigh Inc. |
| Firm location | San Antonio, TX |
| Affected scope | 231 units |
| Distribution | US Nationwide and Middle East |
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-0926-2014) 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? ▼
The Rotoprone therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications. The Rotoprone Therapy System provides up to 62 degrees in both prone and supine positions as well as Trendelenburg/Reverse Trendelenburg positioning. Product Usage: Use of the Rotoprone Therapy System is indicated for patients with severe acute respiratory distress syndrome (ARDS). These are critical patients who are at higher risk of cardiac arrest and mortality. Placing a patient in the prone position may reopen collapsed airways and thus improve pulmonary gas exchange and respiratory mechanics.. Recalled by ArjoHuntleigh Inc.. Units affected: 231 units.
Why was this product recalled? ▼
The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to prone a patient
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 12, 2014. Severity: Moderate. Recall number: Z-0926-2014.
Where was the recalled product distributed? ▼
Distribution: US Nationwide and Middle East.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0926-2014) 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 February 12, 2014. 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.