PlainRecalls
FDA Devices Moderate Class II Terminated

OnControl Biopsy System Ported Needle Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow OnControl Bone Marrow Biopsy System is intended for bone marrow core biopsy of the anterior or posterior iliac crest of adult patients

Reported: December 7, 2016 Initiated: November 8, 2016 #Z-0678-2017

Product Description

OnControl Biopsy System Ported Needle Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow OnControl Bone Marrow Biopsy System is intended for bone marrow core biopsy of the anterior or posterior iliac crest of adult patients

Reason for Recall

Sterility: Due to a potential incomplete seal on the outer sterile package.

Details

Recalling Firm
Teleflex Medical
Distribution
Worldwide Distribution - US (nationwide) Internationally to Brazil, Canada, Ecuador, Guatemala, Mexico and Peru.
Location
Research Triangle Park, NC

Frequently Asked Questions

What product was recalled?
OnControl Biopsy System Ported Needle Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow OnControl Bone Marrow Biopsy System is intended for bone marrow core biopsy of the anterior or posterior iliac crest of adult patients. Recalled by Teleflex Medical.
Why was this product recalled?
Sterility: Due to a potential incomplete seal on the outer sterile package.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 7, 2016. Severity: Moderate. Recall number: Z-0678-2017.