Penner Mfg Inc recalls Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used…

Recall date

January 30, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1306-2015

FDA classification

Class II

Brand / firm

Penner Mfg Inc

Sold / distributed

Worldwide Distribution - USA (nationwide) and Internationally to Canada.

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.