Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-2009-2014)

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 340 SW, 340, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor.

Product Classification:

Class II

Date Initiated: June 5, 2014

Date Posted: July 16, 2014

Recall Number: Z-2009-2014

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: 003-40J, Lot numbers: 177127, 181127, 184127, 225127, 227127, 229127, 231127, 254127, 287127, 291127, 293127, 363127, 364127, 365127, 366127, 367127, 385127, 387127, 389127, 391127, 393127, 423127, 424127, 429127, 431127, 434127, 436127, 437127 & 445127.

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