Z-2269-2015Class II

Prism Medical P-440 Portable Ceiling Lift; PN 303070 and 303070R (refurbished); Patient lift with weight...

Name: Z-2269-2015 Prism Medical P-440 Portable Ceiling Lift; PN 303070 and 303070R (refurbished); Patient lift with weight...
Creator: ErgoSafe Products, LLC (DBA) Prism Medical
Published: 2015-06-24
License: https://open.fda.gov/license/

Handicare USA, Inc. / initiated 2015-06-24 / Terminated

FDA source

ErgoSafe Products, LLC (DBA) Prism Medical began a recall of 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... on 2015-06-24. FDA classified it as Class II and gives the reason as "There is a potential the sling loops may not stay attached to the carry bar hooks". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-2269-2015
Classification: Class II
Status: Terminated
Initiated: 2015-06-24
Posted: 2015-07-27
Terminated: 2017-04-03
Recalling firm: Handicare USA, Inc.
Product: 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.
Product code: FSA Lift, Patient, Non-Ac-Powered
Reason for recall: There is a potential the sling loops may not stay attached to the carry bar hooks.
FDA root cause: Other
Action: Prism Medical sent a Field Safety Notice to affected customers via certified first class US mail. The notice identified the affected product, problem and actions to be taken. For questions contact your local Prism Medical dealer or Prism Medical Customer Service Representative 1-800-891-6502
Quantity in commerce: 7105 lifts
Distribution: Worldwide Distribution - US Nationwide and the countries of:Canada, Great Britain, Australia, South Korea, and Japan.
Product codes and lots: All serial numbers.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2269-2015
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2269-2015	Class II	Terminated	Voluntary: Firm initiated	2015-08-05	2015-07-27
Z-2270-2015	Class II	Terminated	Voluntary: Firm initiated	2015-08-05	2015-07-27

Product code FSA

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)