CLASS II Device recall · Reported 4 May 2016 · FDA Enforcement Report

Spirit One A-C Powered Hospital Bed recalled

Stryker Medical Division of Stryker is recalling Spirit One A-C Powered Hospital Bed, distributed in 19 states. The recall was initiated on 2 Jul 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesMDL#: E341062; Serial Numbers: B5A00-029643 029644 029537 029538 029539 029412 029413 029092 029093 029430 029431 029432 029433 029411 029479 029480 029463 029658 029461 029462 027773 029536 029420 029421 029423 029424 029094 029095 029096 029097 029098 029458 029459 027772 028853 028854 029563 029564 029639 029640 028835 030097 030099 028845 028846 028847 028848 029416 028003 029177 029418 029427 029428 029558 029559 029560 028834 029419 029429 029416 028840 028842 028843 028844 028836 028837 028838 028839 028849 028850 028851 028852 028841 028957 028958 028959 029460 029466 029467 029468 029415 029648 029460 029466 029645 029649 029650 029652 029654 029655 029657 029659 030096 030098 029467 029468 029656 029417 030154 030157 030158 030159 030161 030223 030225 030226 030354 030100 030152 030439; B5F00-029179 028654 028655 028656 028659 028660 028661 028663 028664 028793 028657 029540 029541 029646 029642 028788 029176 029175 029414 029178 029561 028216 029464 030151; B5C00-029182 029183 029184 029185 029186 029187 029188 029189

Quantity recalled143

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1556-2016
FDA event ID: 73131
Recalling firm: Stryker Medical Division of Stryker, Portage, MI
Classification: Class II
Status: Terminated
Recall initiated: 2 Jul 2015
FDA classified: 22 Apr 2016
Reported: 4 May 2016
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Labeling Errors
Device type: Wheelchairs, Beds & Lifts

Timeline

2 Jul 2015	Recall initiated by company
22 Apr 2016	Classified by FDA	+295 days
4 May 2016	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Inaccurate scale systems

Product as listed by the FDA

Spirit One A-C Powered Hospital Bed

Where it was distributed

Distributed in the states of AL, AZ, FL, GA, HI, IA, IL, KS, LA, MI, MN, MO, NE, NJ, OH, PA, SC, TN, and TX, and the countries of Canada and UK.

Alabama Arizona Florida Georgia Hawaii Iowa Illinois Kansas Louisiana Michigan Minnesota Missouri Nebraska New Jersey Ohio Pennsylvania South Carolina Tennessee Texas

Questions about this recall

Why was it recalled?

Inaccurate scale systems

Which lots are affected?

MDL#: E341062; Serial Numbers: B5A00-029643 029644 029537 029538 029539 029412 029413 029092 029093 029430 029431 029432 029433 029411 029479 029480 029463 029658 029461 029462 027773 029536 029420 029421 029423 029424 029094 029095 029096 029097 029098 029458 029459 027772 028853 028854 029563 029564 029639 029640 028835 030097 030099 028845 028846 028847 028848 029416 028003 029177 029418 029427 029428 029558 029559 029560 028834 029419 029429 029416 028840 028842 028843 028844 028836 028837 028838 028839 028849 028850 028851 028852 028841 028957 028958 028959 029460 029466 029467 029468 029415 029648 029460 029466 029645 029649 029650 029652 029654 029655 029657 029659 030096 030098 029467 029468 029656 029417 030154 030157 030158 030159 030161 030223 030225 030226 030354 030100 030152 030439; B5F00-029179 028654 028655 028656 028659 028660 028661 028663 028664 028793 028657 029540 029541 029646 029642 028788 029176 029175 029414 029178 029561 028216 029464 030151; B5C00-029182 029183 029184 029185 029186 029187 029188 029189

Where was it sold?

Distributed in the states of AL, AZ, FL, GA, HI, IA, IL, KS, LA, MI, MN, MO, NE, NJ, OH, PA, SC, TN, and TX, and the countries of Canada and UK.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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