Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported November 2, 2016
ReTurn 7500/7500 Aid, transfer
During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount o…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Handicare USA, Inc. recalled ReTurn 7500/7500 Aid, transfer - a moderate-severity action.
ReTurn 7500/7500 Aid, transfer was recalled by Handicare USA, Inc. in November 2, 2016. Reason: During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, af…. Check the official notice for the remedy. Verify recall #Z-0303-2017 with the FDA Devices before acting.
The recall
Handicare USA, Inc. issued this moderate-severity FDA Devices recall-During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, af….
- Moderate
- severity level
- 29 units
- affected scope
- Class II
- classification
- November 2, 2016
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0303-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0303-2017) was formally reported on November 2, 2016, with the manufacturer initiating the action on April 15, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Handicare USA, Inc. is listed as the recalling firm, operating out of Allentown, PA. Federal records list the affected scope as 29 units , plus 47 wing handles were shipped as spare parts.
The documented reason for this recall is: During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount of play in the attachment of the ladder, … Distribution data in the federal record shows the product reached: US Distribution to the states of : NY, NJ, NV, NE, IL, CT, PA and ME. 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
29 units , plus 47 wing handles were shipped as spare parts
Related Recalls
6
3 from same agency
Product description
ReTurn 7500/7500 Aid, transfer
Reason for recall
During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount of play in the attachment of the ladder, which in turn results in high load at the attachment holes of the ladder. Eventually, this may cause mechanical fatigue in the material of the ladder.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0303-2017 |
| Date reported | November 2, 2016 |
| Date initiated | April 15, 2014 |
| Recalling firm | Handicare USA, Inc. |
| Firm location | Allentown, PA |
| Affected scope | 29 units , plus 47 wing handles were shipped as spare parts |
| Distribution | US Distribution to the states of : NY, NJ, NV, NE, IL, CT, PA and ME |
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-0303-2017) 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? ▼
ReTurn 7500/7500 Aid, transfer. Recalled by Handicare USA, Inc.. Units affected: 29 units , plus 47 wing handles were shipped as spare parts.
Why was this product recalled? ▼
During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount of play in the attachment of the ladder, which in turn results in high load at the attachment holes of the ladder. Eventually, this may cause mechanical fatigue in the material of the ladder.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 2, 2016. Severity: Moderate. Recall number: Z-0303-2017.
Where was the recalled product distributed? ▼
Distribution: US Distribution to the states of : NY, NJ, NV, NE, IL, CT, PA and ME.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0303-2017) 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.
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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 November 2, 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.