FDAClass IIAugust 24, 2016

Valleylab Laparoscopic Flat L-Hook Electrode recall: Sterility Concern

Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code: E2784R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for…

Why was Valleylab Laparoscopic Flat L-Hook Electrode recalled?

Potential for compromise of the package resulting in a breach of the sterile barrier

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?

Affected Lot Range: 209503X through 60870086X

Product
Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code: E2784R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for…
Recalling firm
Medtronic
Quantity
3470
Distribution
Worldwide Distribution - US (nationwide) and Internationally to Australia, Canada, Japan, Korea, Hong Kong, Thailand,
Recall date
August 24, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
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