CLASS II Device recall · Reported 15 Mar 2017 · FDA Enforcement Report

A-series lift - A625 Manual recalled by ErgoSafe Products, LLC (

ErgoSafe Products LLC ( is recalling A-series lift - A625 Manual, distributed in Montana, Nevada, Virginia. The recall was initiated on 30 Jan 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesA6MC000016 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

Quantity recalled76

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-1406-2017
FDA event ID: 76351
Recalling firm: ErgoSafe Products LLC (, Maryland Heights, MO
Classification: Class II
Status: Terminated
Recall initiated: 30 Jan 2017
FDA classified: 3 Mar 2017
Reported: 15 Mar 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Device Malfunction
Device type: Other Medical Devices

Timeline

30 Jan 2017	Recall initiated by company
3 Mar 2017	Classified by FDA	+32 days
15 Mar 2017	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.

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

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

Where it was distributed

Product was distributed to MT and NV; one VA consignee.

Montana Nevada Virginia

Questions about this recall

Why was it recalled?

During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.

Which lots are affected?

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

Where was it sold?

Product was distributed to MT and NV; one VA consignee.

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 76351

Reported	Class	Recall	Company	Reason	Where
15 Mar 2017	CLASS II	A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni recalled	ErgoSafe Products LLC (	Device Malfunction	MT, NV, VA

More recalls from ErgoSafe Products LLC (

All 7

Reported	Class	Recall	Company	Reason	Where
15 Mar 2017Device	CLASS II	A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni recalled	ErgoSafe Products LLC (	Device Malfunction	MT, NV, VA
21 Dec 2016Device	CLASS II	Carry bar which is an accessory to a lift used recalled	ErgoSafe Products LLC (	Foreign Material	Nationwide
25 Nov 2015Device	CLASS II	Prism Medical C-300 Consumer Ceiling Lift recalled	ErgoSafe Products LLC (	Other	Nationwide
25 Nov 2015Device	CLASS II	Prism Medical P-300 Portable Consumer Lift recalled	ErgoSafe Products LLC (	Other	Nationwide
5 Aug 2015Device	CLASS II	Prism Medical P-600 Portable Ceiling Lift recalled	ErgoSafe Products LLC (	Device Malfunction	Nationwide

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All 13,778

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