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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 76351

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
January 30, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
ErgoSafe Products, LLC (DBA) Prism Medical

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.

Z-1405-2017
Recall number
Z-1405-2017
Initiated
January 30, 2017
Classification
Class II
Status
Terminated
Quantity
21

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

A6MC000110 A6M0001010 A6M0001011 A6M0001012 A6M0001013 A6M0001014 A6M0001015 A6M0001016 A6M0001017 A6M0001018 A6M0001019 A6M0001020 A6M0001021 A6M0001025 A6M0001026 A6M0001029 A6M0001022 A6M0001023 A6M0001024 A6M0001027 A6M0001028

Distribution pattern

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

device · product 2 of 2

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

Z-1406-2017
Recall number
Z-1406-2017
Initiated
January 30, 2017
Classification
Class II
Status
Terminated
Quantity
76

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

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