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U.S. Department of Health and Human Services

Class 2 Device Recall Unifine Pentips 5mm x 31G pen needles

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 Class 2 Device Recall Unifine Pentips 5mm x 31G pen needlessee related information
Date Initiated by FirmNovember 06, 2017
Create DateJanuary 17, 2018
Recall Status1 Terminated 3 on February 12, 2021
Recall NumberZ-0381-2018
Recall Event ID 78483
510(K)NumberK152339 
Product Classification Needle, hypodermic, single lumen - Product Code FMI
ProductUnifine 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.
Code Information UPC #384703550018: Batch No. AN 3550, Lot No. 1705722.S846; Batch No. AN 3550AC, Lot No. 1705122.S929.  
Recalling Firm/
Manufacturer
Owen Mumford USA, Inc.
1755 W Oak Commons Ct
Marietta GA 30062-2280
For Additional Information ContactTravis Shaw
770-977-2226
Manufacturer Reason
for Recall
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.
FDA Determined
Cause 2
Environmental control
ActionOwen 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.
Quantity in Commerce2,660 cartons (266,000 pen needles)
DistributionUS 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
Total Product Life CycleTPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = FMI
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