FDA Devices recall · Reported April 1, 2015
Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used with Whirlpool or Aqua-Aire (air bubbling) bathing system intended for use in nursing homes, hospitals, and assisted living facilities to transfer and/or lift patients under the direct supervision of trained staff. Model 392000-1 is equipped with a scale.
If the patient sits on either wing, not squarely on the center section of the Stretcher Lift, tipping and injury to the operator or patient could result. The device manual was upd…
Penner Mfg Inc recalled Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific… - a moderate-severity action.
Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific… was recalled by Penner Mfg Inc in April 1, 2015. Reason: If the patient sits on either wing, not squarely on the center section of the Stretcher Lift, tipping and inj…. Check the official notice for the remedy. Verify recall #Z-1306-2015 with the FDA Devices before acting.
The recall
Penner Mfg Inc issued this moderate-severity FDA Devices recall-If the patient sits on either wing, not squarely on the center section of the Stretcher Lift, tipping and inj….
- Moderate
- severity level
- 158 units
- affected scope
- Class II
- classification
- April 1, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1306-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1306-2015) was formally reported on April 1, 2015, with the manufacturer initiating the action on January 30, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Penner Mfg Inc is listed as the recalling firm, operating out of Aurora, NE. Federal records list the affected scope as 158.
The documented reason for this recall is: If the patient sits on either wing, not squarely on the center section of the Stretcher Lift, tipping and injury to the operator or patient could result. The device manual was updated with an additional warning statemen… Distribution data in the federal record shows the product reached: Worldwide Distribution - USA (nationwide) and Internationally to Canada.. 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, 6 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 - 40,861 medical devices recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.
Product description
Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used with Whirlpool or Aqua-Aire (air bubbling) bathing system intended for use in nursing homes, hospitals, and assisted living facilities to transfer and/or lift patients under the direct supervision of trained staff. Model 392000-1 is equipped with a scale.
Reason for recall
If the patient sits on either wing, not squarely on the center section of the Stretcher Lift, tipping and injury to the operator or patient could result. The device manual was updated with an additional warning statement.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1306-2015 |
| Date reported | April 1, 2015 |
| Date initiated | January 30, 2015 |
| Recalling firm | Penner Mfg Inc |
| Firm location | Aurora, NE |
| Affected scope | 158 |
| Distribution | Worldwide Distribution - USA (nationwide) and Internationally to Canada. |
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-1306-2015) 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.
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Nationwide recalls with similar severity or category timing
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Similar severity · nearest report date
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Methodology · Corrections · Archive as of August 2026