FDA Recall Terminated

Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic, non-pyrogenic, single use pen needles for the subcutaneous injection of drugs from pen injectors.

Recall: Z-0381-2018 · Initiated November 6, 2017

Recall

Recall Number
Z-0381-2018
Event Number
78483
Firm
Owen Mumford USA, Inc.
FEI Number
1000219614
Product Code
FMI
Status
Terminated
Root Cause
Environmental control
Initiated
November 6, 2017
Terminated
February 12, 2021
Address
1755 W Oak Commons Ct, Marietta, GA, 30062-2280

Description

Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic, non-pyrogenic, single use pen needles for the subcutaneous injection of drugs from pen injectors.

Reason

Device may potentially be compromised by water in end user packaging. Exposure to liquid may compromise sterility. This may appear as discoloring or yellowing of the device's protective seal.

Action

Owen Mumford sent an Urgent Medical Device Recall Notification letter dated November 6, 2017 via email. The letter identified the affected product, problem and actions to be taken. The letter instructed customers to check inventory for affected product, contact the Customer Service Department to arrange return of affected product, complete and return the response form and to either provide a customer list for Owen and Mumford to notify their customers or confirmation that they will notify their customers if further distributed.

Distribution

US Nationwide Distribution in the states of AL, AZ, CA, CO, FL, GA, HI, IA, IL, MA, MI, MN, MO, MS, NC, NH NJ, NY, OH, OK, PA, TN, NX, UT, VA, VT, WA, WV

Quantity

2,660 cartons (266,000 pen needles)