Devices

Device Recall Penner

  • Model / Serial
    Serial numbers: 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, 04061028102, 04061028103, 04061028104, 04061028105, 04081009901, 04091187201, 04111563801, 04111568501, 05071272201, 05071272202, 05071272203, 05071272204, 05071272205, 05081019501, 05091197901, 05091197902, 05091201301, 05111513201, 05111576501, 05121762001, 06050840801, 06050840802, 06050840803, 06050840804, 06050840805, 06050840806, 06081037501, 06081039402, 06081039403, 06101394201, 07071320201, 07071320202, 07071328501, 07071328502, 07071328503, 07091223901, 07091223902, 07101410901, 07101415901, 08040660501, 08040660502, 08061090801, 08061090802, 08061090803, 08061090804, 08101430502, 08101439601, 09081073301, 09081074401, 09081076501, 09101453401, 09101457101, 09111641101, 09111641301, 10061121201, 10061121202, 10061121203, 10061121204, 10071396601, 10071396602, 10071396603, 10071396604, 10101463201, 10101464701, 10111652001, 11040710501, 11040710502, 11040710503, 11040710504, 11040710505, 11040710506, 11040710507, 11040710508, 11040710601, 11040710602, 11040710603, 11040710604, 11040710605, 11040710606, 11040710607, 11040710608, 11081101401, 11081105901, 11081113501, 11091285601, 11091285602, 11101475201, 11101476201, 11101476401, 11101477901, 11101478101, 12101495201, 12111677201, 12111686301, 12111686302, 12111688401, 03121734201S, 04040581301A
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) and Internationally to Canada.
  • 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.
  • Manufacturer
    Penner Mfg Inc
  • 1 Event

Manufacturer

Penner Mfg Inc
  • Manufacturer Address
    Penner Mfg Inc, 102 Grant St Ste A, Aurora NE 68818-3200
  • Source
    USFDA

13 devices with a similar name

Learn more about the data here

Device Recall Penner Patient Transfer/Lift System
  • Model / Serial
    Model 380000-1 - Serial numbers 08020346201, 8020346203, 10020360901, 10020360902, 10020360903, and 08020346202;  Model 380000-2 - Serial numbers 08020346201, 08020346203, and 11020367501.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide distribution: USA and countries including: Canada and Mexico.
  • Product Description
    Penner Manufacturing Patient Transfer/Lift System, Cascade Transfer, Models 380000-1 (white) and 380000-2 (gray). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. || For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.
  • Manufacturer
    Penner Mfg Inc
Device Recall Penner Patient Transfer/Lift System
  • Model / Serial
    Model 382000-1 - Serial numbers 07030456102, 05030435303, 07030456101, 07030456103, 05030435301, 09030479202, 09030479201, 09030479205, 11030501601, 07030456104, 11030501602, 11030501604, 12030507602, 12030507601, 12030507603, 11030501603, 09030479203, 12030507604, 11030501605, 12030509803, 07030435302, 12030509802, 12030507605, 12030509805, 01040535102, 01040535103, 06040623302, 06040623303, 01040535101, 06040623304, 07040635502, 07040635501, 07040635503, 06040623301, 07040635504, 07040635505, 07040635506, 07040635601, 07040635602, 07040635603, 07040635604, 08040665602, 07040635605, 08040665601, 07040635606, 08040665603, 08040665604, 12030509804, 08040665605, 09040678702, 09040678701, 09040678703, 09040678704, 11040712001, 11040712002, 11040712003, 11040712004, 11040712005, 01050741002, 01050741003, 01050741004, 01050741005, 02050756702, 02050756704, 02050756701, 03050798302, 03050798305, 03050790404, 02050756703, 03050798301, 03050790402, 03050798304, 03050790401, 03050798303, 03050790403, 06050840201, 06050840202,  06050840203, 06050840204, 06050840205, 06050840206, 06050840207, 03050790405, 06050840209, 08050884101, 06050840210, 08050884401, 08050884404, 10050924102, 10050924101, 10050924103, 10050924106, 11050939502, 10050924105, 11050939503, 10050924104, 11050939601, 11050939501, 11050939504, 11050939603, 11050939604, 02060988902, 11050939602, 02060988903, 06061061801, 02060988904, 02060988901, 06061061804, 09061105901, 08050884403, 08061096702, 08061096703, 10061134503, 06071297106, 07071328104, 06050840208, and 01050741001.   Model 382000-1L - Serial numbers 03050798604, 03050798602, 2050756901, 03050798601, 06050845901, 03050798603, 06050867102, 08050884701, 06050845902, 06050867104, 06050867103, 08050884702, 08050884703, 08050884704, 01060954301, 01060971601, 01060954302, 01060971604, 01060971602, 01060971603, 02060989001, 02060989002, 06050867101, 02060989004, 02060989003, 02060989005, 02060989006, 06061061901, and 06061061902.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide distribution: USA and countries including: Canada and Mexico.
  • Product Description
    Penner Manufacturing Transfer Electric Cascade Patient Transfer/Lift System, Models 382000-1 (right entry) and 382000-1L (left entry). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. || For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.
  • Manufacturer
    Penner Mfg Inc
Device Recall Penner Patient Transfer/Lift System
  • Model / Serial
    Serial numbers 09050908201, 11050949102, 09050908203, 09050908204, 01060954501, 11050949103, 01060954503, 01060954502, 01060954504, and 01060954505.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide distribution: USA and countries including: Canada and Mexico.
  • Product Description
    Penner Manufacturing Bariatric Patient Transfer/Lift System, Cascade Transfer, Models 382500-1 (right entry). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. || For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.
  • Manufacturer
    Penner Mfg Inc
Device Recall Penner Patient Transfer/Lift System
  • Model / Serial
    Model 383000-1 - Serial numbers 06030440001, 06030447201, 06030447202, 06030447204, 06030447205, 06030440002, 09030473801, 09030473802, 09030473804, 06030447203, 09030479101, 09030473803, 09030473806, 09030479102, 09030473805, 09030479103, 09030479104, 09030479105, 09030483202, 09030483204, 09030483201, 11030504803, 11030504801, 11030504802, 11030504804, 11030504805, 01040534301, 12030507701, 12030507702, 12030507703, 12030507704, 12030507705, 01040534302, 01040534303, 09030483203, 01040535201, 01040535202, 01040535203, 01040535204, 01040535205, 03040549001, 03040549002, 03040549006, 03040549003, 03040549004, 03040549005, 03040578002, 03040578001, 03040578004, 06040607702, 06040607703, 06040607705, 06040607701, 06040607801, 06040607802, 06040607803, 06040607804, 06040607805, 05040590801, 05040590802, 05040590803, 05040590804, 05040590805, 05040590806, 06040623403, 06040623401, 06040623404, 06040623402, 06040623405, 09040678801, 09040678804, 09040678806, 09040678803, 09040678805, 03040578003, 09040678807, 11040711901, 11040711902, 11040711903, 11040711904, 01050737401, 09040678802, 01050737402, 01050737403, 01050737405, 01050737404, 01050737406, 02050756801, 02050756802, 02050762601, 02050756805, 02050762602, 02050782001, 02050762604, 02050782002, 02050782003, 02050782004, 02050762603, 03050798201, 03050798202, 03050798203, 03050798205, 03050798207, 03050798208, 03050798206, 03050798204, 06050841002, 06050841001, 03050798209, 06050841004, 03050798210, 06050841003, 07050872001, 07050872003, 02050762605, 07050872002, 07050872004, 08050884503, 08050884601, 08050884504, 08050884501, 08050884502, 10050924003, 10050924004, 10050924005, 10050924001, 08050884602, 10050924002, 11050939702, 08050884604, 11050939703, 08050884603, 11050939701, 01060954201, 10050924006, 11050939704, 01060954202, 01060954203, 01060954204, 01060954205, 02060998904, 02060998902, 02060998901, 01060954206, 02060998903, 02060998905, 02060998906, 04061024901, 04061024902, 04061024903, 04061024904, 04061024905, 06061062003, 06061062004, 06061062005, 06061062006, 04061024906, 06061062001, 06061062002, 02071210003, and 03080991702.  Model 383000-1L - 06050846002, 02050757001, 02050757002, 03050798701, 03050798703, 03050798702, 03050798704, 06050846001, 06050867202, 06050867201, 06050867203, 06050867204, 09050903601, 09050903603, 09050903602, 09050907601, 09050907603, 09050907604,  09050907602, 11050934501, 11050934502, 11050934504, 11050934503, 01060954401, 03061010201, 01060954404, 01060954402, 03061010202, 01060954403, 03061010203, 04061025002, 03061010204, 04061025001, 04061025003, 02080971502, 02080971503, and 10061134802.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide distribution: USA and countries including: Canada and Mexico.
  • Product Description
    Penner Manufacturing Transfer Electric Cascade with Scale, Patient Transfer/Lift System, Models 383000-1 (right entry) and 383000-1L (left entry). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. || For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.
  • Manufacturer
    Penner Mfg Inc
Device Recall Penner Patient Transfer/Lift System
  • Model / Serial
    Serial numbers 02060996003, 02060996005, 11050949101, 02060996002, 11050949104, 02060996004, 03061002801, 03061002802, 03061002805, 03061002803, 03061002804, 05061039201, 05061039202, 05061039203, 05061039204, 05061039205, 06061062101, 06061062102, 06061062103, and 06061062104
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide distribution: USA and countries including: Canada and Mexico.
  • Product Description
    Penner Manufacturing Transfer Electric Bariatric with Scale, Patient Transfer/Lift System, Cascade Transfer, Models 383500-1 (right entry with scale). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. || For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.
  • Manufacturer
    Penner Mfg Inc
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