Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported August 5, 2015
Prism Medical P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specification of 600 lbs (273 kg). Product Usage: The P-600 lift is a lifting aid used by health care professionals and those providing care in the home to lift, position, and transfer clients or a disabled family member. The ceiling lift makes it possible to move mobility impaired individuals with minimal strain or risk to the caregiver, while providing complete safety, dignity, and comfort for the client or fa
There is a potential the sling loops may not stay attached to the carry bar hooks.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
ErgoSafe Products, LLC (DBA) Prism Medical recalled Prism Medical P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specificat… - a moderate-severity action.
Prism Medical P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specificat… was recalled by ErgoSafe Products, LLC (DBA) Prism Medical in August 5, 2015. Reason: There is a potential the sling loops may not stay attached to the carry bar hooks.. Check the official notice for the remedy. Verify recall #Z-2270-2015 with the FDA Devices before acting.
The recall
ErgoSafe Products, LLC (DBA) Prism Medical issued this moderate-severity FDA Devices recall-There is a potential the sling loops may not stay attached to the carry bar hooks..
- Moderate
- severity level
- Class II
- classification
- August 5, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2270-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2270-2015) was formally reported on August 5, 2015, with the manufacturer initiating the action on June 24, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. ErgoSafe Products, LLC (DBA) Prism Medical is listed as the recalling firm, operating out of Maryland Heights, MO. Federal records list the affected scope as 409 lifts.
The documented reason for this recall is: There is a potential the sling loops may not stay attached to the carry bar hooks. Distribution data in the federal record shows the product reached: Worldwide Distribution - US Nationwide and the countries of:Canada, Great Britain, Australia, South Korea, and Japan.. 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
409 lifts
Related Recalls
6
3 from same agency
Product description
Prism Medical P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specification of 600 lbs (273 kg). Product Usage: The P-600 lift is a lifting aid used by health care professionals and those providing care in the home to lift, position, and transfer clients or a disabled family member. The ceiling lift makes it possible to move mobility impaired individuals with minimal strain or risk to the caregiver, while providing complete safety, dignity, and comfort for the client or family member.
Reason for recall
There is a potential the sling loops may not stay attached to the carry bar hooks.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2270-2015 |
| Date reported | August 5, 2015 |
| Date initiated | June 24, 2015 |
| Recalling firm | ErgoSafe Products, LLC (DBA) Prism Medical |
| Firm location | Maryland Heights, MO |
| Affected scope | 409 lifts |
| Distribution | Worldwide Distribution - US Nationwide and the countries of:Canada, Great Britain, Australia, South Korea, and Japan. |
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-2270-2015) 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 P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specification of 600 lbs (273 kg). Product Usage: The P-600 lift is a lifting aid used by health care professionals and those providing care in the home to lift, position, and transfer clients or a disabled family member. The ceiling lift makes it possible to move mobility impaired individuals with minimal strain or risk to the caregiver, while providing complete safety, dignity, and comfort for the client or family member.. Recalled by ErgoSafe Products, LLC (DBA) Prism Medical. Units affected: 409 lifts.
Why was this product recalled? ▼
There is a potential the sling loops may not stay attached to the carry bar hooks.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 5, 2015. Severity: Moderate. Recall number: Z-2270-2015.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - US Nationwide and the countries of:Canada, Great Britain, Australia, South Korea, and Japan..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2270-2015) 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 August 5, 2015. 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.