Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-2010-2014)

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:

Aqua 540 SW, 540 w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.

Product Classification:

Class II

Date Initiated: June 5, 2014

Date Posted: July 16, 2014

Recall Number: Z-2010-2014

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: 005-40, Lot numbers: 001125, 002125, 003125, 004125, 005125, 006125, 007125, 008125, 009125, 010125, 011125, 012125, 013125, 014125, 015125, 016125, 017125, 019125, 020125, 021125, 022125, 023125, 024125, 025125, 026125 & 032125.

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