FDA Device recall Z-0190-2014
Sterrad 100NX, Product Code: 10104
- FDA Device
- Class II
- terminated
- Published 2013-11-20
On 2013-11-20 the FDA classified a Class II recall of Sterrad 100NX, Product Code: 10104 by Advanced Sterilization Products, citing advanced Sterilization Products (ASP) is recalling the Sterrad 100NX Sterilizer some healthcare workers detected odors/smells emanating from the 100NX Sterilizers, and it may be r….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0190-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-18 |
| Published | 2013-11-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Advanced Sterilization Products |
| Distribution | US |
Product
Sterrad 100NX, Product Code: 10104. Used to sterilize heat and moisture sensitive reusable medical devices.
Reason
Advanced Sterilization Products (ASP) is recalling the Sterrad 100NX Sterilizer some healthcare workers detected odors/smells emanating from the 100NX Sterilizers, and it may be related to normal breakdown of the oil used in the Sterrad 200 vacuum pumps.
Identifiers
| code_info | Batch 1041070019 1041080059 1041080056 1041080058 1041080055 1041080064 1041080063 1041080057 1041080060…Batch 1041070019 1041080059 1041080056 1041080058 1041080055 1041080064 1041080063 1041080057 1041080060 1041070023 1041070022 1041080069 1041080070 1041080066 1041080068 1041080072 1041080073 1041080082 1041080077 1041080061 1041080074 1041080076 1041080078 1041080079 1041080081 1041080087 1041080071 1041080093 1041080080 1041080095 1041080090 1041080089 1041080088 1041080097 1041080098 1041080091 1041080099 1041080100 1041080101 1041080096 1041080159 1041080103 1041080102 1041080104 1041080160 1041080167 1041080172 1041080168 1041080169 1041080174 1041070049 1041070051 1041070048 1041080083 1041080086 1041080165 1041080173 1041080175 1041080164 1041080163 1041080180 1041080084 1041080182 1041080184 1041080189 1041080186 1041080191 1041080178 1041080177 1041080179 1041080185 1041080193 1041080197 1041080199 1041080188 1041080195 1041080198 1041080215 1041080194 1041080214 1041080260 104108020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0190-2014%22
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