Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 18, 2017
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear premature…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Handicare Usa Inc recalled PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered - a moderate-severity action.
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered was recalled by Handicare Usa Inc in October 18, 2017. Reason: During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts ma…. Check the official notice for the remedy. Verify recall #Z-0013-2018 with the FDA Devices before acting.
The recall
Handicare Usa Inc issued this moderate-severity FDA Devices recall-During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts ma….
- Moderate
- severity level
- 8 units
- affected scope
- Class II
- classification
- October 18, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0013-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0013-2018) was formally reported on October 18, 2017, with the manufacturer initiating the action on September 8, 2017. 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 Maryland Heights, MO. Federal records list the affected scope as 8 units.
The documented reason for this recall is: During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear prematurely at max load (625 lbs). We have identi… Distribution data in the federal record shows the product reached: Us and Canada. 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
8 units
Related Recalls
6
3 from same agency
Product description
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Reason for recall
During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear prematurely at max load (625 lbs). We have identified the root cause as a supplied component that was not to specification. If the strap wears during use there is a potential risk for the person being supported by the lift to drop.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0013-2018 |
| Date reported | October 18, 2017 |
| Date initiated | September 8, 2017 |
| Recalling firm | Handicare Usa Inc |
| Firm location | Maryland Heights, MO |
| Affected scope | 8 units |
| Distribution | Us and Canada |
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-0013-2018) 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? ▼
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered. Recalled by Handicare Usa Inc. Units affected: 8 units.
Why was this product recalled? ▼
During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear prematurely at max load (625 lbs). We have identified the root cause as a supplied component that was not to specification. If the strap wears during use there is a potential risk for the person being supported by the lift to drop.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 18, 2017. Severity: Moderate. Recall number: Z-0013-2018.
Where was the recalled product distributed? ▼
Distribution: Us and Canada.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0013-2018) 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 October 18, 2017. 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.