FDAClass IISeptember 20, 2017

BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile recall: Foreign Material

BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose…

Why was BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile recalled?

Presence of loose polypropylene foreign matter above release specification.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Numbers: 6211579, 6271695, 6154760, 6154765 & 5268868

Product
BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose…
Recalling firm
Becton Dickinson & Company
Quantity
1,249,200 units
Distribution
US Distribution to: TX, PA, VA, CA, NY, IL, MI, NC, SC and KS.
Recall date
September 20, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls