Reported Apr 1, 2015 · Terminated

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

Penner Mfg Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Penner Mfg Inc · 102 Grant St Ste A · Aurora, NE · 68818-3200

Is this the product you have?

  • 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.
Lot codes and dates
  • Serial numbers

    158 of 158 codes

    • 01050741201
    • 01071198001
    • 01071198002
    • 01071198003
    • 01071198004
    • 01091136401
    • 01091136402
    • 01091136403
    • 01101314201
    • 01101322801
    • 01111505901
    • 02071228401
    • 02071228402
    • 02071228403
    • 02071228404
    • 02080975001
    • 02080975002
    • 02091137801
    • 02091149801
    • 02121713401
    • 03050791101
    • 03050804301
    • 03050804302
    • 03050804303
    • 03050804304
    • 03050804305
    • 03050804306
    • 03071247201
    • 03071247202
    • 03071247203
    • 03071247204
    • 03080984601
    • 03080984602
    • 03080984603
    • 03091161601
    • 03101347201
    • 03121742801
    • 03122862901
    • 04040581301
    • 04040581302
    • 04040581303
    • 04040581304
    • 04040581305
    • 04040581306
    • 04040581307
    • 04040581308
    • 04040581310
    • 04040581311
    • 04040581312
    • 04040581313
    • 04040581314
    • 04040586101
    • 04050810401
    • 04050810402
    • 04050810403
    • 04050810404
    • 04050810406
    • 04050810408
    • 04050810410
    • 04061028101
Amount recalled
158

Where it was sold

  • Nationwide

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 10, 2016 · Data as of Sep 19, 6:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.