FDA Device recall Z-2340-2014
FANFOLD DRAPE - CUSTOMED (1) DRAPE SHEET 42" X 57" SMS (1) WRAPPER 24" X 24" EO sterilized surgical convenient packs packaged into polyeste…
- FDA Device
- Class I
- terminated
- Published 2014-09-10
On 2014-09-10 the FDA classified a Class I recall of FANFOLD DRAPE - CUSTOMED (1) DRAPE SHEET 42" X 57" SMS (1) WRAPPER 24" X 24" EO sterilized surgical convenient packs packaged into polyeste… by Customed, citing customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to t….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2340-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-05-20 |
| Published | 2014-09-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Customed |
| Distribution | US |
Product
FANFOLD DRAPE - CUSTOMED (1) DRAPE SHEET 42" X 57" SMS (1) WRAPPER 24" X 24" EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.
Reason
Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.
Identifiers
| code_info | Product code 900-633, 56 lots: 109020284 109040849 109051210 109071550 109092075 109102340 109112583 109122699…Product code 900-633, 56 lots: 109020284 109040849 109051210 109071550 109092075 109102340 109112583 109122699 110010102 110010242 110020460 110030683 110030781 110041029 110051365 110071704 110082030 110092351 110102554 110102670 110122940 111010146 111020229 111030685 111040913 111051394 111051461 111061682 111061683 111071941 111071967 111082323 111092606 111102772 112041342 112052001 112062213 112062502 112083438 112093948 113036375 113036674 113036735 113047026 113057496 113068177 113078605 113089078 113099293 113109865 131110269 131210834 140211674 140412471 140412797 140513350 |
|---|
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-2340-2014%22
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