Home › Device types › LTZ
Condom With Nonoxynol-9
FDA product code LTZ · Class 2 · Obstetrics/Gynecology
0
Registered devices
10
Adverse events
1
Recalls
22
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2002-11-25 | Ansell Healthcare Inc | The condoms are being recalled because information recently available indicates some of these condoms do not meet airburst test standards |
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