Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-2004-2014)

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 640 SW, 650, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .

Product Classification:

Class II

Date Initiated: June 5, 2014

Date Posted: July 16, 2014

Recall Number: Z-2004-2014

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: 400640, Lot numbers: 021126, 022126, 030126, 031126, 032126, 033126, 034126, 037126, 038126, 039126, 040126, 047126, 048126, 049126, 050126, 051126, 052126, 059126, 060126, 061126, 066126, 067126, 072126, 073126, 074126, 081126, 082126, 083126, 084126, 085126, 093126, 094126, 095126, 096126, 100126, 101126, 102126, 103126, 104126, 109126, 110126, 116126, 117126, 118126, 119126, 125126, 126126, 127126 & 151126.

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