FDAClass IIJuly 22, 2015

Dual Delivery 4DD-1 of GYC-1000 Green Laser recall

Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green Laser Photocoagulator Model GYC- 1000 is indicated for…

Why was Dual Delivery 4DD-1 of GYC-1000 Green Laser recalled?

Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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?

Model GYC4DD-1

Product
Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green Laser Photocoagulator Model GYC- 1000 is indicated for…
Recalling firm
Nidek Inc
Quantity
22 units
Distribution
US Distribution to the states of : CA, IL, MN, MO, OR, IL, UT RI, MA, WA, NE, NY, NJ, TX and WI.
Recall date
July 22, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
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