FDAClass IINovember 29, 2017

Medline Pedi Elbow Closed Suction Catheter recall

MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER, 8Fr, REF DYNCPE8

Why was Medline Pedi Elbow Closed Suction Catheter recalled?

Products labeled as sterile were distributed prior to sterilization

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 2861707008

Product
MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER, 8Fr, REF DYNCPE8
Recalling firm
Medline Industries Inc
Quantity
190 units
Distribution
FL, IN, TN, GA, NJ, UT, MD, Nicaragua, Honduras
Recall date
November 29, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls