Stryker Recalls Spirit One Hospital Beds Due to Inaccurate Scale Systems
Stryker is recalling 143 Spirit One A-C Powered Hospital Beds because their scale systems are inaccurate. The beds were distributed in 19 US states, Canada, and the UK.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves inaccurate scale systems without reported injuries or illnesses, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Stryker Medical Division of Stryker Corporation is recalling 143 units of the Spirit One A-C Powered Hospital Bed. The recall was initiated because the scale systems in these beds are inaccurate.
The affected beds were distributed in the states of Alabama, Arizona, Florida, Georgia, Hawaii, Iowa, Illinois, Kansas, Louisiana, Michigan, Minnesota, Missouri, Nebraska, New Jersey, Ohio, Pennsylvania, South Carolina, Tennessee, and Texas, as well as in Canada and the United Kingdom. The specific units are identified by MDL number E341062 and a list of serial numbers provided in the recall notice.
Healthcare facilities and consumers should stop using the affected beds and contact Stryker for further instructions on the recall process.
The recalled product
- Product
- Spirit One A-C Powered Hospital Bed
- Manufacturer
- Stryker Medical Division of Stryker Corporation
- Category
- Medical Device — Hospital Bed
- Hazard
- Affected units
- 143
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- MDL#: E341062
- B5C00-029182 029183 029184 029185 029186 029187 029188 029189
Distribution
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