CLASS II Device recall · Reported 5 Aug 2015 · FDA Enforcement Report
Prism Medical P-440 Portable Ceiling Lift recalled
ErgoSafe Products LLC ( is recalling Prism Medical P-440 Portable Ceiling Lift, distributed nationwide in the US. The recall was initiated on 24 Jun 2015 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2269-2015
- FDA event ID
- 71376
- Recalling firm
- ErgoSafe Products LLC (, Maryland Heights, MO
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 24 Jun 2015
- FDA classified
- 27 Jul 2015
- Reported
- 5 Aug 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 24 Jun 2015 | Recall initiated by company | |
| 27 Jul 2015 | Classified by FDA | +33 days |
| 5 Aug 2015 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
There is a potential the sling loops may not stay attached to the carry bar hooks.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Prism Medical P-440 Portable Ceiling Lift; PN 303070 and 303070R (refurbished); Patient lift with weight specification of 440 lbs (200 kg). Product Usage: The P-440 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.
Where it was distributed
Worldwide Distribution - US Nationwide and the countries of:Canada, Great Britain, Australia, South Korea, and Japan.
Questions about this recall
Why was it recalled?
There is a potential the sling loops may not stay attached to the carry bar hooks.
Which lots are affected?
All serial numbers.
Where was it sold?
Worldwide Distribution - US Nationwide and the countries of:Canada, Great Britain, Australia, South Korea, and Japan.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 71376| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Prism Medical P-600 Portable Ceiling Lift recalled | ErgoSafe Products LLC ( | Device Malfunction | Nationwide |
More recalls from ErgoSafe Products LLC (
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni recalled | ErgoSafe Products LLC ( | Device Malfunction | MT, NV, VA |
| Device | CLASS II | A-series lift - A625 Manual recalled by ErgoSafe Products, LLC ( | ErgoSafe Products LLC ( | Device Malfunction | MT, NV, VA |
| Device | CLASS II | Carry bar which is an accessory to a lift used recalled | ErgoSafe Products LLC ( | Foreign Material | Nationwide |
| Device | CLASS II | Prism Medical C-300 Consumer Ceiling Lift recalled | ErgoSafe Products LLC ( | Other | Nationwide |
| Device | CLASS II | Prism Medical P-300 Portable Consumer Lift recalled | ErgoSafe Products LLC ( | Other | Nationwide |
Other Wheelchairs, Beds & Lifts recalls
All 172| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge 2.0 (ilevel) recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |