FDAClass IINovember 5, 2014

Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer recall

Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.

Why was Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer recalled?

CooperSurgical is recalling two lots of 900-863 because the wrong package insert (IFU) was placed into the shipper.

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?

Lots 149460 and 149911

Product
Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.
Recalling firm
CooperSurgical, Inc. D.B.A. Lone Star Medical Products
Quantity
90 units
Distribution
Worldwide Distribution: US (nationwide) to North Carolina; and Internationally to Australia and Italy.
Recall date
November 5, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls