Drug recall

ADAPTOR, 040 HUM, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of…

FDA recall event 70280 · Class II · Teleflex Medical

Key facts

Event ID 70280
Recall numbers Z-1095-2015, Z-1096-2015, Z-1097-2015, Z-1098-2015, Z-1099-2015, Z-1100-2015, Z-1101-2015, Z-1102-2015, Z-1103-2015, Z-1104-2015, Z-1105-2015, Z-1106-2015 and 3 more
Recalling firm Teleflex Medical
Product type Devices
Products ADAPTOR, 040 HUM, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to…, AQUA 540 SW, 540 W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor…, AQUAPAK 101 SW, 190ML W/040 ADAPTOR, JAPA Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of…, AQUAPAK 340 SW, 340 ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of…, AQUAPAK 340 SW, 340ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of… and 9 more
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall The packages may contain foreign material (black particles).
Initiation date Jan 14, 2015
Report date Feb 18, 2015
Termination date Dec 4, 2017
City Research Triangle Park
State NC
Country United States
FEI number 1044475

At a glance

  • 10–99 Products in this recall
  • None FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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