ICU Medical, Inc.: Medical Device Recall in 2014 - (Recall #: Z-2293-2014)

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:

CAP Change Kit w/MicroClave Clear, Item No. B78109 BD prefilled syringes are co-packaged into a kit with ICU devices and other components. The affected lots are easily identifiable via the lot number printed on the pouch.

Product Classification:

Class II

Date Initiated: August 5, 2014

Date Posted: August 27, 2014

Recall Number: Z-2293-2014

Event ID: 68973

Reason for Recall:

ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially product sterility.

Status: Terminated

Product Quantity: 300 units

Code Information:

Lot No. 2704633, 2705206

Distribution Pattern:

Nationwide Distribution - USA including AL and MD.

Voluntary or Mandated:

Voluntary: Firm initiated