Z-0381-2018 Class II Terminated
FDA device recall Z-0381-2018 was initiated by Owen Mumford USA, Inc. on November 6, 2017 and is designated Class II. 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. The recall status is terminated (terminated February 12, 2021). Affected quantity: 2,660 cartons (266,000 pen needles).
Recall Details
- Product Type
- Devices
- Report Date
- January 24, 2018
- Initiation Date
- November 6, 2017
- Termination Date
- February 12, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,660 cartons (266,000 pen needles)
Product 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 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.
Distribution Pattern
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
Code Information
UPC #384703550018: Batch No. AN 3550, Lot No. 1705722.S846; Batch No. AN 3550AC, Lot No. 1705122.S929.