FDAClass IIJune 13, 2018

3910-090-800 ASSY recall

3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of…

Why was 3910-090-800 ASSY recalled?

Inadvertent shipment of expired units.

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 No. 14239AG2, UPC 07613327055795. The expiration date marked on the box is August 2018, but it should be August 2016.

Product
3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of…
Recalling firm
Stryker Corporation
Quantity
2 boxes (5 units per box)
Distribution
US distribution to Massachusetts only..
Recall date
June 13, 2018
Classification
Class II
Status
Completed
Agency
FDA (device)
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