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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71015

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
April 14, 2015
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Nihon Kohden America Inc

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

1 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 1

Remote Network Station, Catalog RNS-9703, Model No. RNS-9703-19, RNS-9703-24, Software version 02.40. The RNS 9703 is intended for use by medical professionals to provide secondary cardiac and vital signs monitoring for multiple patients within a medical facility. The device will display physiological data from up to 16 telemetry receiver/transmitters or bedside monitors and generate an alarm when a measured parameter falls outside a pre-set limit or when life threatening arrhythmias are detected.

Z-1543-2015
Recall number
Z-1543-2015
Initiated
April 14, 2015
Classification
Class II
Status
Terminated
Recalling firm
Nihon Kohden America Inc
Quantity
208 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Nihon Kohden America (NKA) is recalling the Remote Network Station (RNS) 9703 because it may fail to sound.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Nihon Kohden America (NKA) is recalling the Remote Network Station (RNS) 9703 because it may fail to sound.

Code information

RNS-9703-019 Serial Number 2002 and higher RNS-9703-024 Serial Number 2002 and higher Serial number 2040 2041 2042 2043 2044 2045 2014 2015 2016 2017 2030 2031 2060 2061 2062 2067 2068 2069 2070 2033 2095 2096 2097 2098 2029 2036 2039 2041 2042 2043 2044 2045 2046 2047 2048 2049 2123 2011 2012 2013 2022 2023 2024 2025 2026 2027 2028 2032 2037 2106 2037 2038 2010 2077 2078 2034 2035 2021 2022 2023 2024 2028 2029 2059 2060 2061 2062 2063 2002 2063 2064 2065 2105 2066 2006 2007 2099 2109 2110 2030 2031 2050 2051 2052 2053 2054 2055 2056 2057 2058 2032 2046 2047 2048 2049 2050 2051 2052 2053 2054 2055 2056 2057 2058 2059 2064 2065 2066 2067 2068 2069 2070 2071 2072 2073 2074 2075 2076 2077 2078 2079 2080 2081 2082 2083 2084 2085 2086 2087 2088 2089 2090 2091 2092 2093 2094 2095 2096 2097 2098 2099 2100 2101 2102 2103 2104 2100 2009 2111 2112 2113 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2071 2072 2073 2074 2075 2018 2019 2033 2034 2036 2101 2086 2087 2088 2089 2080 2081 2082 2083 2084 2085 2025 2026 2027 2038 2039 2021 2003 2004 2005 2020 2090 2091 2092 2093 2094 2008

Distribution pattern

US Distribution to states of: AL, CO, DE, FL, GA, HI, KY, IL, IN, MA, MD, MI, MN, MO, NC,, ND, NJ, NY.OH, PA, and WV.