FDA Enforcement Class II Terminated

Container fill and transfer sets, 250 mL, 500 mL, 1000 mL, 2000 mL, 3000 mL, or 4000 mL.

Recall: Z-2260-2016 · Reported August 3, 2016

Enforcement

Recall Number
Z-2260-2016
Event ID
74043
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
The Metrix Company
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 3, 2016
Initiation Date
June 23, 2016
Classification Date
July 22, 2016
Termination Date
April 11, 2023
Address
4400 Chavenelle Rd, N/A, Dubuque, IA, 52002-2655, United States

Description

Container fill and transfer sets, 250 mL, 500 mL, 1000 mL, 2000 mL, 3000 mL, or 4000 mL.

Reason

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.

Code Info

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: 58781, 58785, 62005, 62010, 62015, 62025, 62030, 62035, 64005, 64010, 64015, 64025, 64030, 64035, 64781, 65005, 65010, 65015, 65025, 65030, 65035, 66005, 66010, 66015, 66020, 66025, 66030, 66035, 66305, 66310, 66315, 66325, 66330, 66335, 66705, 66710, 66715, 66725, 66730, 66735, 66910, 66915, 66925, 66930, 66935, 67005, 67010, 67015, 67025, 67030, 67035, 69005, 69010, 69015, 69025, 69030, 69035

Distribution

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

Quantity

137,598 cases