Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-2007-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Aquapak SW/EAU, Sterile, 340 mL, w/Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.

Product Classification:

Class II

Date Initiated: June 5, 2014

Date Posted: July 16, 2014

Recall Number: Z-2007-2014

Event ID: 68493

Reason for Recall:

The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.

Status: Terminated

Product Quantity: 7,758,650 ea. (total for all types listed)

Code Information:

Product Code: 003-40C, Lot numbers: 109127, 155127, 157127, 174127, 195127, 222127, 277127, 335127, 337127, 384127, 422127, 425127, 497127 & 500127.

Distribution Pattern:

Worldwide Distribution-USA (nationwide) and the countries of Belgium, Canada, China, Germany, Great Britain, France, India, Malaysia, Mexico, Philippines, Singapore, Thailand and Zambia.

Voluntary or Mandated:

Voluntary: Firm initiated