Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported August 3, 2016
Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of wheelchair's intended use is to provide mobility to persons limited to a sitting position.
There is an observed failure of the backrest bracket which can fatigue over the life time of the product. When this occurs there is the possibility of the bracket fracturing caus…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Sunrise Medical (US) LLC recalled Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of wheelch… - a moderate-severity action.
Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of wheelch… was recalled by Sunrise Medical (US) LLC in August 3, 2016. Reason: There is an observed failure of the backrest bracket which can fatigue over the life time of the product. Whe…. Check the official notice for the remedy. Verify recall #Z-2290-2016 with the FDA Devices before acting.
The recall
Sunrise Medical (US) LLC issued this moderate-severity FDA Devices recall-There is an observed failure of the backrest bracket which can fatigue over the life time of the product. Whe….
- Moderate
- severity level
- 12K units
- affected scope
- Class II
- classification
- August 3, 2016
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2290-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2290-2016) was formally reported on August 3, 2016, with the manufacturer initiating the action on July 1, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Sunrise Medical (US) LLC is listed as the recalling firm, operating out of Fresno, CA. Federal records list the affected scope as 12,142 devices in US, 1,710 devices internationally..
The documented reason for this recall is: There is an observed failure of the backrest bracket which can fatigue over the life time of the product. When this occurs there is the possibility of the bracket fracturing causing the backrest to detach from the chai… Distribution data in the federal record shows the product reached: US and Mexico, Japan, Chile, Kuwait, Columbia, Hong Kong, China, Uruguay, South Africa, Costa Rica, South Korea, Singapore, New Zealand, El Salvador, Bahrain, Uruguay, Lebanon, United Arab Emirates, Brazil, Argentina…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
12,142 devices in US, 1,710 devices internationally.
Related Recalls
6
3 from same agency
Product description
Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of wheelchair's intended use is to provide mobility to persons limited to a sitting position.
Reason for recall
There is an observed failure of the backrest bracket which can fatigue over the life time of the product. When this occurs there is the possibility of the bracket fracturing causing the backrest to detach from the chair frame.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2290-2016 |
| Date reported | August 3, 2016 |
| Date initiated | July 1, 2016 |
| Recalling firm | Sunrise Medical (US) LLC |
| Firm location | Fresno, CA |
| Affected scope | 12,142 devices in US, 1,710 devices internationally. |
| Distribution | US and Mexico, Japan, Chile, Kuwait, Columbia, Hong Kong, China, Uruguay, South Africa, Costa Rica, South Korea, Singapore, New Zealand, El Salvador, Bahrain, Uruguay, Lebanon, United Arab Emirates, Brazil, Argentina, Netherlands Antill… |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2290-2016) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of wheelchair's intended use is to provide mobility to persons limited to a sitting position.. Recalled by Sunrise Medical (US) LLC. Units affected: 12,142 devices in US, 1,710 devices internationally..
Why was this product recalled? ▼
There is an observed failure of the backrest bracket which can fatigue over the life time of the product. When this occurs there is the possibility of the bracket fracturing causing the backrest to detach from the chair frame.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 3, 2016. Severity: Moderate. Recall number: Z-2290-2016.
Where was the recalled product distributed? ▼
Distribution: US and Mexico, Japan, Chile, Kuwait, Columbia, Hong Kong, China, Uruguay, South Africa, Costa Rica, South Korea, Singapore, New Zealand, El Salvador, Bahrain, Uruguay, Lebanon, United Arab Emirates, Brazil, Argentina, Netherlands Antilles, British Virgin Islands,.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2290-2016) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported August 3, 2016. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.