Drug recall
Adaptor, 040 Hum, International, Teleflex Medical, respiratory gas humidifier adaptor.
FDA recall event 68493 · Class II · Teleflex Medical
Key facts
| Event ID | 68493 |
|---|---|
| Recall numbers | Z-2003-2014, Z-2004-2014, Z-2005-2014, Z-2006-2014, Z-2007-2014, Z-2008-2014, Z-2009-2014, Z-2010-2014, Z-2011-2014, Z-2012-2014, Z-2013-2014, Z-2014-2014 and 3 more |
| Recalling firm | Teleflex Medical |
| Product type | Devices |
| Products | Adaptor, 040 Hum, International, Teleflex Medical, respiratory gas humidifier adaptor., Aqua 540 SW, 540 w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor., Aquapak 101 SW, 190, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor, Aquapak 340 SW, 340, mL w/040 Adaptor, French, Teleflex Medical, respiratory gas humidifier adaptor., Aquapak 340 SW, 340, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor . and 10 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The seals of the adaptor packaging may be creased which may potentially affect packaging integrity., The seals of the respiratory gas humidifier adaptor packaging may be creased which may potentially affect packaging integrity. |
| Initiation date | Jun 5, 2014 |
| Report date | Jul 16, 2014 |
| Termination date | Jul 2, 2015 |
| City | Durham |
| State | NC |
| Country | United States |
| FEI number | 3005747797 |
At a glance
- 10–99 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: