Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Recalled by Penner Mfg Inc Due to If the patient sits on either wing, not...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Penner Mfg Inc directly.
Affected Products
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.
Quantity: 158
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Penner Mfg Inc
Penner Mfg Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report