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U.S. Department of Health and Human Services

Class 2 Device Recall Bausch & Lomb Millennium Microsurgical System

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  Class 2 Device Recall Bausch & Lomb Millennium Microsurgical System see related information
Date Initiated by Firm January 15, 2010
Date Posted May 26, 2010
Recall Status1 Terminated 3 on May 17, 2013
Recall Number Z-1663-2010
Recall Event ID 54268
510(K)Number K961310  
Product Classification instrument, vitreous aspiration and cutting, ac-powered cord - Product Code NFJ
Product Bausch & Lomb Millennium Microsurgical System.
Code Information All devices manufactured since 2004
Recalling Firm/
Manufacturer		 Bausch & Lomb Inc
1400 North Goodman Street
Rochester NY 14609-3547
For Additional Information Contact Chris Willis
585-338-6000
Manufacturer Reason
for Recall		 The AC power cords used on these products are subject to an FDA Alert -- Safety Investigation of Certain Medical Device Power Cords: Initial Communication, Date Issued: October 19, 2009.
FDA Determined
Cause 2		 Nonconforming Material/Component
Action A "URGENT: POWER CORD RECALL" letter and copies of the FDA Alert dated Oct. 19, 2009 were sent to all customers on or about Jan. 15, 2010, by Stericycle, a recall notification service. The letter describes the product, problem and actions to be taken by the customers as well as FDA's recommendations and actions. The customers were made aware of the FDA Alert concerning the AC power cords and notified that these power cords were used in the devices. They were requested to inspect the power cords for damage and notify the recalling firm if damage is noted or if they have experienced sparking, charring, or firing from the power cords and/or cracking or failure of the prongs. In the absence of those conditions, customers were given the option of returning the power cord for replacement and/or during the regularly scheduled servicing of the device. If you would like a new power cord, please contact Customer Service at 1-800-338-2020 for a free replacement.
Quantity in Commerce Quantity never provided by firm
Distribution Worldwide distribution: United States & Puerto Rico; Venezuela, India, Trinidad and Tobago, Colombia, Sri Lanka, Hong Kong, Vietnam, and Peru.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = NFJ and Original Applicant = STORZ INSTRUMENT CO.
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