FDA Device recall Z-2375-2015
Wall Chart for STERRAD 100NX System, P/N 10104
- FDA Device
- Class II
- terminated
- Published 2015-08-19
On 2015-08-19 the FDA classified a Class II recall of Wall Chart for STERRAD 100NX System, P/N 10104 by Advanced Sterilization Products, citing advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for STERRAD 100NX System because it incorrectly states "APTIMAX Instrument Trays can be enclosed in either polypr….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2375-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-17 |
| Published | 2015-08-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Advanced Sterilization Products |
| Distribution | US |
Product
Wall Chart for STERRAD 100NX System, P/N 10104. The STERRAD 100NX Sterilizer is designed for sterilization of both metal and nonmetal medical devices at low temperatures.
Reason
Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for STERRAD 100NX System because it incorrectly states "APTIMAX Instrument Trays can be enclosed in either polypropylene wrap or in Tyvek Pouches with STERRAD Chemical Indicators."
Identifiers
| code_info | 1041110428 1041110429 1043141347 1043130246 1041100160 1041100193 1043140260 1041110040 1041120389 1041110125…1041110428 1041110429 1043141347 1043130246 1041100160 1041100193 1043140260 1041110040 1041120389 1041110125 1043150133 1041090452 1041120062 1041130103 1041070049 1041100128 1043141230 1041100228 1041110512 1041080260 1041100245 1041100325 1041100327 1041100328 1041110513 1043141014 1041080059 1041120039 1043141234 1041110214 1041120483 1041110516 1041120099 1043140161 1043140298 1041100218 1041080204 1043150029 1041120098 1041120108 1041120334 1043141214 1043141222 1041090297 1041120050 1041120051 1043140068 1041090307 1041100235 1041110411 1043141042 1041100219 1041090328 1041110137 1041130401 1041090293 1043150141 10104001070042 10104001070043 1041120390 10104001080074 1041130188 1041130009 1041080082 10104001080031 1041130067 1041130070 10104001080092 1041080188 1041110119 1041120488 1043140137 1041130229 1041090298 1041120061 1041120075 1041120077 1041100288 1041100292 1041080226 1041090350 10411101 |
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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-2375-2015%22
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