Allergan Medical Optics Inc Surgical Tubing Pack, Model: AMO Prestige Pack, Product Code OPO40 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Surgical Tubing Pack, Model: AMO Prestige Pack, Product Code OPO40
Brand
Allergan Medical Optics Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot # Exp. date 3JR190 10/2006 3KR128 11/2006 3LR100 12/2006 3MR002 12/2006 3MR047 12/2006 3MR048 12/2006 3MR081 01/2007 3MR082 01/2007 4AR045 01/2007 4AR050 01/2007 4AR058 01/2007
Allergan Medical Optics Inc is recalling Surgical Tubing Pack, Model: AMO Prestige Pack, Product Code OPO40 due to The lots are being recalled because the tray lid may not be adequately sealed under the red arrow in the upper right corner of the package tray. The . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The lots are being recalled because the tray lid may not be adequately sealed under the red arrow in the upper right corner of the package tray. The blue wrapping within the tray may not be sterile and may pose a potential risk of infection to the patient if used in a sterile field.
Recommended Action
Per FDA guidance
On March 31, 2004, a product notification letter was mailed to all customers via certified mail. The customers were instructed to stop using, quarantine and return all units. They were instructed to complete the Facsimile form provided and faxed it to the AMO Customer Service at 888-324-0021. They were also instructed to call AMO Customer Service at 800-366-6554 to make arrangement to return the product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026