Owen Mumford USA, Inc. Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
Brand
Owen Mumford USA, Inc.
Lot Codes / Batch Numbers
Lot numbers: 20V4001.Z3999, Lot 20V4001.Z4019 and 20V4001.Z411
Products Sold
Lot numbers: 20V4001.Z3999, Lot 20V4001.Z4019 and 20V4001.Z411
Owen Mumford USA, Inc. is recalling Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remove due to Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been mixed into a packed configuration of Unifine Pentips Plus 8mm pen needles.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been mixed into a packed configuration of Unifine Pentips Plus 8mm pen needles.
Recommended Action
Per FDA guidance
The firm sent an e-mail on 05/06/2019 to all the distributors. The distributors were directed to quarantine all affected product and contact the company for return. Distributors were also directed to cease distribution and contact their customers (Pharmacies) with recall notification with instructions to contact Owen Mumford with product return, if any on hand..
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026