FDA Recall Terminated

VISU 200 on S8 Floor Stand, Manufactured by Carl Zeiss Surgical GmbH, Germany Medical device: Surgical microscope used during ophthalmic surgeries, which allows real time visualization of the surgical area. Product Quantity Distributed (Int) 2540 units

Recall: Z-0904-2011 · Initiated May 18, 2009

Recall

Recall Number
Z-0904-2011
Event Number
52716
Firm
Carl Zeiss Meditec Inc
FEI Number
2918630
Product Code
EPT
Status
Terminated
Root Cause
Labeling mix-ups
Initiated
May 18, 2009
Posted
January 14, 2011
Terminated
February 9, 2011
Address
5160 Hacienda Dr, Dublin, CA, 94568

Description

VISU 200 on S8 Floor Stand, Manufactured by Carl Zeiss Surgical GmbH, Germany Medical device: Surgical microscope used during ophthalmic surgeries, which allows real time visualization of the surgical area. Product Quantity Distributed (Int) 2540 units

Reason

Potential Retina Damage-- An error in the user manual may result in misapplied filter and injury during treatment.

Action

Carl Zeiss Meditec Inc sent a SAFETY ALERT letter dated May 18, 2009, via Federal Express to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were reminded to use the correct retinal protection filter (GG475) when using the OPMI VISU 200 system during ophthalmic surgery. Verify the position of the retinal protection filter and inform their staff of the customizable feature. Verify that the correct filter was in place. Customers were asked to complete the acknowledgement form indicating receipt of the alert. Sign and return the form to: Carl Zeiss Meditec in Dublin, California via the enclosed self-addressed, pre-paid Federal Express envelope. For any questions customers should call (925) 557-4422.

Distribution

Worldwide Distribution including USA (nationwide) and the UK

Quantity

2540 units