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Staarvisic II recallZ-1106-05 · Staar Surgical Co Inc · initiated Jul 18, 2005

Terminated All recalls posted in August 2005

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Staar Surgical Co Inc or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Sterility may be compromised.

FDA root cause category: Other

What the company is doing

Recall will be communicated by telephone, email and letter. A fax back form will be used to track response and to identify ammount on hand.

Recall details

Recall number
Z-1106-05
Recall class
Not yet classified by the FDA
Status
Terminated
Initiated by the company
Jul 18, 2005
Posted by the FDA
Aug 6, 2005
Recalling firm
Staar Surgical Co Inc
Quantity
16,464
Product code
LZP
FDA submissions
P000046
Distribution
Nationwide, Canada and Puerto Rico

Product description

Staarvisic II Sodium Hyaluronate, 0.8 mL

Code information (models, lots, serial numbers)

Lot B041118C Exp Date 12/31/2005

Other devices under the same FDA submission

2 devices cleared under P000046 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Sources and updates

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