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U.S. Department of Health and Human Services

Class 2 Device Recall Bausch & Lomb Millennium TSV 25 Ga. High Speed Posterior Vitrectomy Pack, CX4925

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  Class 2 Device Recall Bausch & Lomb Millennium TSV 25 Ga. High Speed Posterior Vitrectomy Pack, CX4925 see related information
Date Initiated by Firm February 09, 2007
Date Posted April 21, 2007
Recall Status1 Terminated 3 on April 07, 2009
Recall Number Z-0766-2007
Recall Event ID 37281
510(K)Number K980488  
Product Classification Vitrectomy Cutter - Product Code HQE
Product Bausch & Lomb Millennium TSV 25 Ga. High Speed Posterior Vitrectomy Pack, Catalog No: CX4925, containing 1/25-ga. cutter along with accessories, RX. The firm names on the label are Bausch & Lomb Incorporated, Rochester, NY, and Bausch & Lomb Incorporated, Kingston-upon-Thames, UK.
Code Information All lots
Recalling Firm/
Manufacturer		 Bausch & Lomb Inc
1400 North Goodman Street
Rochester NY 14609-3547
For Additional Information Contact Douglas J. Fortunato
585-338-5477
Manufacturer Reason
for Recall		 The cutter probe tip breaks during use.
FDA Determined
Cause 2		 Other
Action On 2/12/07, express mail letters were addressed to operating room supervisors to notify them of the recall. Additional E-mail notifications were issued on 2/14/07 to doctors and letters were addressed to them on 2/20/07 to make them aware of the recall, although they do not directly receive the product. The communications instructed them to not use the affected product and to return it, along with the business reply card.
Quantity in Commerce 13,685 units of Catalog No: CX4925
Distribution Class II Recall - Worldwide Distribution --- USA including states of MO, NC, FL, CA, and TX and countries of Canada, China, Japan, Australia, Hong Kong, India, Singapore, Korea, Taiwan, Thailand, Argentina, Brazil, Mexico, and The Netherlands
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 = HQE and Original Applicant = STORZ INSTRUMENT CO.
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