Z-1406-2017Class II

A-series lift - A625 Manual Part No. 324117. Prism Medical

Name: Z-1406-2017 A-series lift - A625 Manual Part No. 324117. Prism Medical
Creator: ErgoSafe Products, LLC (DBA) Prism Medical
Published: 2017-01-30
License: https://open.fda.gov/license/

Handicare USA, Inc. / initiated 2017-01-30 / Terminated / root cause: design

FDA source

ErgoSafe Products, LLC (DBA) Prism Medical began a recall of A-series lift - A625 Manual Part No. 324117. Prism Medical on 2017-01-30. FDA classified it as Class II and gives the reason as "During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-1406-2017
Classification: Class II
Status: Terminated
Initiated: 2017-01-30
Posted: 2017-02-28
Terminated: 2017-12-04
Recalling firm: Handicare USA, Inc.
Product: A-series lift - A625 Manual Part No. 324117. Prism Medical.
Product code: FSA Lift, Patient, Non-Ac-Powered
Reason for recall: During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Root cause tag: design
FDA root cause: Device Design
Action: The recalling firm called each customer on Jan 30, 2017 to review the recall and schedule a time for the firm to come to their facility to personally swap the recalled product for a new device. The FSNs were sent on Jan 31, 2017.
Quantity in commerce: 76
Distribution: Product was distributed to MT and NV; one VA consignee.
Product codes and lots: A6MC000016 A6MC000019 A6MC000020 A6MC000021 A6MC000022 A6MC000023 A6MC000024 A6MC000025 A6MC000026 A6MC000027 A6MC000028 A6MC000029 A6MC000030 A6MC000031 A6MC000009 A6MC000002 A6MC000004 A6MC000001 A6MC000003 A6MC000005 A6MC000006 A6MC000007 A6MC000008 A6MC000010 A6MC000011 A6MC000012 A6MC000013 A6MC000014 A6MC000015 A6MC000017 A6MC000018 A6MC000096 A6MC000087 A6MC000088 A6MC000090 A6MC000091 A6MC000092 A6MC000093 A6MC000094 A6MC000048 A6MC000068 A6MC000070 A6MC000072 A6MC000073 A6MC000074 A6MC000075 A6MC000078 A6MC000079 A6MC000081 A6MC000082 A6MC000083 A6MC000085 A6MC000086 A6MC000042 A6MC000043 A6MC000045 A6MC000046 A6MC000047 A6MC000049 A6MC000050 A6MC000051 A6MC000052 A6MC000053 A6MC000054 A6MC000055 A6MC000056 A6MC000057 A6MC000058 A6MC000059 A6MC000060 A6MC000061 A6MC000062 A6MC000063 A6MC000064 A6MC000066 A6MC000071

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1406-2017
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1405-2017	Class II	Terminated	Voluntary: Firm initiated	2017-03-15	2017-03-03
Z-1406-2017	Class II	Terminated	Voluntary: Firm initiated	2017-03-15	2017-03-03

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)