Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
Summary
The FDA issued a Class II for Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built by Owen Mumford USA, Inc.. Reason: 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..
Details
Source
Device Recall
External ID
Z-2078-2021
Action Date
2021-07-21
Status
Ongoing
Category
device
Product Description
Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
Lot/Code Info: Lot numbers: 20V4001.Z3999, Lot 20V4001.Z4019 and 20V4001.Z411
Quantity Affected: 2,593 cartons of 100 ea.
Reason for Recall
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.
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, TX, UT, VA, VT, WA, and WV.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-05-26
Company
Marietta, GA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 157 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Owen Mumford USA, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Owen Mumford USA, Inc. have FDA actions?
This is the only FDA action we have on record for Owen Mumford USA, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2078-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
Want to know the moment something like this happens?
Get alerts for deviceRelated Actions
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 888810200
Covidien LP · 2023-08-23
Sterile Procedural Trays, labeled as the following: a. BREAST AUGMENTATION b. BREAST REDUCTION CDS c. CUH ABDOMINO
MEDLINE INDUSTRIES, LP - Northfield · 2023-02-15
VTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the uri
Boston Scientific Corporation · 2024-09-25
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoo
Enchroma Inc · 2024-11-27
Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;
Adept Medical Ltd · 2025-01-29