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Owen Mumford USA Recalls
7 recalls on record · April 8, 2015 to July 21, 2021 · Medical Devices
Recalls by year
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21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 21, 2021Medical DevicesFDA
Owen Mumford USA, Inc. recalls Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
Hazard: 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.
November 13, 2019Medical DevicesFDA
Owen Mumford USA, Inc. recalls Petfine Auto Injector, REF 3310VET
Hazard: There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107
November 13, 2019Medical DevicesFDA
Owen Mumford USA, Inc. recalls Autoject EI, REF AJ1310
Hazard: There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107
January 24, 2018Medical DevicesFDA
Owen Mumford USA, Inc. recalls Unifine Pentips 5mm x 31G pen needles, packaged in 30 ct pen needles. Product Usage: Sterile, non-toxic, non-pyroge
Hazard: 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.
January 24, 2018Medical DevicesFDA
Owen Mumford USA, Inc. recalls Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic, non-pyroge
Hazard: 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.
July 22, 2015Medical DevicesFDA
Owen Mumford USA, Inc. recalls Autopen Classic Automatic insulin delivery pen, 3.0ml x 2 unit 2-42 units, AN3800, Lot 7JH, NDC 08470-3800-01, The pr
Hazard: The dials in the Autopens are not working - the dial does not stay dialed, but springs right back to 0. As a result, the patient could not dial up a dose of medicine to deliver via an injection.
April 8, 2015Medical DevicesFDA
Owen Mumford USA, Inc. recalls Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by pa
Hazard: The syringe carrier is missing components: a damper and spring.