Stryker Recalls Spirit One A-C Powered Hospital Beds Due to Brake Faults
Stryker is recalling 143 Spirit One A-C Powered Hospital Beds because of customer complaints regarding a faulty brake system.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a faulty brake system on a hospital bed, which poses a risk of harm to patients, although no specific injuries or illnesses are reported in the source text.
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 due to customer complaints associated with a faulty brake system.
The affected units were distributed to hospitals and healthcare facilities in the United States and internationally. In the US, distribution included 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. The products were also distributed to Canada and the United Kingdom.
Healthcare facilities should stop using the affected beds and contact Stryker for instructions on how to proceed. The specific serial numbers affected are listed in the official recall documentation.
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
Related recalls
Same manufacturer · Stryker Medical Division of Stryker Corporation
See all →- ModerateStryker Cub pediatric cribs sold in USA missing two warning labels
FDA (Devices) · 2026-03-25
- ModerateBariatric hospital beds recalled because they are not tested with certain mattresses
FDA (Devices) · 2025-12-17
- ModerateHospital mattresses recalled because they are not tested with certain beds
FDA (Devices) · 2025-12-17
- HighProCurity patient beds recalled for electrical safety testing defects
FDA (Devices) · 2023-12-13
- HighProCuity Hospital Patient Beds Recalled for Missing Electrical Safety Testing
FDA (Devices) · 2023-12-13
Same hazard · brake failure
See all →- SevereFord Recalls ABS Modules With Incorrect Software Programming
NHTSA · 2026-10-20
- Severe
- Severe
- SevereNova Bus Recalls 2024-2025 LFS Transit Buses for Parking Brake Defect
NHTSA · 2026-09-22
- Severe
Similar recalls
- ModerateStryker Recalls Spirit One Hospital Beds Due to Inaccurate Scale Systems
FDA (Devices) · 2016-05-04
- HighStryker Recalls Spirit Plus Hospital Beds Due to Actuator Failure
FDA (Devices) · 2016-08-10
- HighStryker Recalls Spirit Select and Plus Hospital Beds Due to Actuator Failure
FDA (Devices) · 2016-08-10
- HighStryker Spirit Plus Bed Recall for Potential Entrapment Risk
FDA (Devices) · 2018-11-21
- HighStryker Spirit Select Bed Recall for Potential Entrapment Risk
FDA (Devices) · 2018-11-21
- HighStryker Recalls Performance-LOAD Ambulance Cot Fasteners Due to Fastening Issues
FDA (Devices) · 2016-12-21