Sunrise Medical Recalls Six Quickie Q7 Adult Rigid Wheelchairs
Sunrise Medical is recalling six Quickie Q7 Adult Rigid Wheelchairs because the height-adjustable handle may dislodge due to failing locking mechanisms.
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 involves a risk-of-harm product (wheelchair handle dislodgement) where no specific injuries or illnesses have been reported in the source text, fitting the criteria for a High severity score.
Plain-English summary
Sunrise Medical (US) LLC is recalling six units of the Quickie Q7 Adult Rigid Wheelchair Model EIR4. The recall was initiated because the height-adjustable handle on these specific chairs has the potential to dislodge due to failing locking mechanisms.
The affected units were distributed nationwide in the states of Colorado and Maine. The specific serial numbers for the recalled chairs are R4-025066, R4-025051, R4-025010, R4-024771, R4-024738, and R4-024649.
Consumers who own one of these specific serial numbers should contact Sunrise Medical (US) LLC for further instructions on how to resolve the issue.
The recalled product
- Product
- Quickie Q7 Adult Rigid Wheelchair Model EIR4.
- Manufacturer
- Sunrise Medical (US) LLC
- Category
- Medical Device — Mobility Aids
- Affected units
- 6
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 (6)
- Serial numbers: R4-025066
- R4-025051
- R4-025010
- R4-024771
- R4-024738
- R4-024649.
Distribution
Part of a larger recall action
This product is one of 2 recalled by Sunrise Medical (US) LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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