FDA recall record

ErgoSafe Products, LLC (DBA) Prism Medical Prism Medical P-440 Portable Ceiling Lift recall — FDA Z-2269-2015

There is a potential the sling loops may not stay attached to the carry bar hooks.

Class IIclassification
Z-2269-2015official record ID
Aug 5, 2015report date

Recall record at a glance

Official recordZ-2269-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmErgoSafe Products, LLC (DBA) Prism Medical
Report dateAug 5, 2015
Recall initiation dateJun 24, 2015
Quantity7105 lifts
LocationMaryland Heights, MO, United States

Official product description

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.

Why the product was recalled

There is a potential the sling loops may not stay attached to the carry bar hooks.

Distribution information

Worldwide Distribution - US Nationwide and the countries of:Canada, Great Britain, Australia, South Korea, and Japan.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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