FDA Device recall Z-2692-2016

UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Catalog No. 775222 UniCel DxH Slidemaker Stainer (DxH SMS) Instructions for…

FDA Device
Class II
terminated
Published 2016-09-07

On 2016-09-07 the FDA classified a Class II recall of UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Catalog No. 775222 UniCel DxH Slidemaker Stainer (DxH SMS) Instructions for… by Beckman Coulter, citing beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System to reduce the potential for flammable liquids coming into contact with electrical c….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2692-2016
Classification	Class II
Status	terminated
Initiated	2016-08-04
Published	2016-09-07
Last updated	2026-09-13 11:54 UTC
Company	Beckman Coulter
Distribution	US

Product

UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Catalog No. 775222 UniCel DxH Slidemaker Stainer (DxH SMS) Instructions for Use (IFU) Part Number B26647AC The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a whole-blood sample, smears a blood film on a clean microscope slide, and delivers a variety of fixatives, stains, buffers, and rinse solutions to that blood smear

Reason

Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System to reduce the potential for flammable liquids coming into contact with electrical components in the Stainer module possibly causing a fire.

Identifiers

code_info	AZ28094 AW01001 AY01010 AY04011 AW20069 AV14059 AZ12033 AZ12034 AZ06021 AY52153 AV01003 AT40021 AV22105 AV… AZ28094 AW01001 AY01010 AY04011 AW20069 AV14059 AZ12033 AZ12034 AZ06021 AY52153 AV01003 AT40021 AV22105 AV12048 AZ12039 AU01015 AU40218 AU40217 AV22099 AU36203 AU36202 AV01012 AW35121 AW35120 AY08031 AU40222 AU11071 AV01008 AY52154 AY52152 AY23080 AV16090 AT49047 AV42151 AV44158 AY10040 AW20067 AW16061 AU40221 AU11070 AW28093 AW10045 AV16079 AV14065 AU01032 AV10042 AU49257 AZ08032 AW23075 AY17061 AY17063 AW35124 AU21134 AW42129 AW20065 AY04013 AU14087 AV48179 AV49181 AW49163 AY01009 AZ22072 AW01010 AU19114 AT35018 AT35017 AT40020 AV06026 AV06030 AY19075 AU08046 AU29170 AU01027 AT49051 AV49183 AZ02004 AZ06022 AU43236 AU20131 AU01005 AU01004 AV01016 AU14086 AW01015 AW06026 AW06024 AV16085 AU01029 AZ02010 AU19116 AZ22073 AZ22074 AZ12041 AZ12042 AZ25090 AZ28091 AY30082 AY30083 AY10054 AY10037 AY04015 AY32106 AY10055 AV01005 AU23152 AU28154 AY35118 AU20123 AU36204 AU13078 AW45141 A

code_info

AZ28094 AW01001 AY01010 AY04011 AW20069 AV14059 AZ12033 AZ12034 AZ06021 AY52153 AV01003 AT40021 AV22105 AV…

AZ28094 AW01001 AY01010 AY04011 AW20069 AV14059 AZ12033 AZ12034 AZ06021 AY52153 AV01003 AT40021 AV22105 AV12048 AZ12039 AU01015 AU40218 AU40217 AV22099 AU36203 AU36202 AV01012 AW35121 AW35120 AY08031 AU40222 AU11071 AV01008 AY52154 AY52152 AY23080 AV16090 AT49047 AV42151 AV44158 AY10040 AW20067 AW16061 AU40221 AU11070 AW28093 AW10045 AV16079 AV14065 AU01032 AV10042 AU49257 AZ08032 AW23075 AY17061 AY17063 AW35124 AU21134 AW42129 AW20065 AY04013 AU14087 AV48179 AV49181 AW49163 AY01009 AZ22072 AW01010 AU19114 AT35018 AT35017 AT40020 AV06026 AV06030 AY19075 AU08046 AU29170 AU01027 AT49051 AV49183 AZ02004 AZ06022 AU43236 AU20131 AU01005 AU01004 AV01016 AU14086 AW01015 AW06026 AW06024 AV16085 AU01029 AZ02010 AU19116 AZ22073 AZ22074 AZ12041 AZ12042 AZ25090 AZ28091 AY30082 AY30083 AY10054 AY10037 AY04015 AY32106 AY10055 AV01005 AU23152 AU28154 AY35118 AU20123 AU36204 AU13078 AW45141 A

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2692-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.