The Metrix Company: Medical Device Recall in 2016 - (Recall #: Z-2262-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Dual Chamber Container fill and transfer sets, 250 mL / 1250 mL or 500 mL / 2500 mL

Product Classification:

Class II

Date Initiated: June 23, 2016

Date Posted: August 3, 2016

Recall Number: Z-2262-2016

Event ID: 74043

Reason for Recall:

An issue was identified after a redesign of the auto compounding device. The compounder cannot meet the designed accuracy specification when dispensing into bags. After reviewing the initial design of the device, it was determined the dispensing volume validation was not properly done and none of the compounders on the market can meet the stated specifications.

Status: Terminated

Product Quantity: 3,829 cases

Code Information:

All lots are being recalled. Lot code consists of the five digit product code followed by a dash followed by a unique five character numeric or alphanumeric sequence. Affected product codes for this product: 58733 and 58734

Distribution Pattern:

Product distributed to medical facilities in the following US states: AL, AZ, CA, CO, CT, FL, IA, IL, KS, LA, MA, MD, MN, NC, OH, PA, PR, TN, TX, UT, and WA. Product was also distributed internationally to the following countries: Australia, Canada, Dominican Republic, Malaysia, Turkey, and United Kingdom

Voluntary or Mandated:

Voluntary: Firm initiated