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U.S. Department of Health and Human Services

Class 2 Device Recall Apple Medical Corporation

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 Class 2 Device Recall Apple Medical Corporationsee related information
Date Initiated by FirmMarch 10, 2006
Date PostedApril 06, 2006
Recall Status1 Terminated 3 on March 07, 2016
Recall NumberZ-0615-06
Recall Event ID 34810
510(K)NumberK961460 
Product Classification Electrocautery, Gynecologic (And Accessories) - Product Code HGI
ProductFischer Cone Biopsy Excisor - Medium Model: 900-151
Code Information Lot Numbers:  D201704, A2002, D201705, D201703, D205001 D209315, D211317, D218412, D217007, D220314, D224801, D224801, D232202 D301327, D302105, D304805, C143E, C213G, D307906, D093H, D311206, D313506 E193A, D316304, D318111, H213A, I153B I153, J073A, J283A, K063M, L043A, L153O A024, A134E
Recalling Firm/
Manufacturer		 Apple Medical Corporation
28 Lord Rd Ste 135
Marlborough MA 01752-4549
For Additional Information ContactJohn C. Pulford
508-624-4645
Manufacturer Reason
for Recall		Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.
FDA Determined
Cause 2		Other
ActionApple Medical Corporation issued letters dated March 21, 2006 to direct accounts and distributors via US Mail. Distributors are requested to sub-recall. Product is to be returned to the firm and destroyed.
Quantity in Commerce2,813.0 boxes
DistributionNationwide Foreign: Australia, Austria, Taiwan, England, FInland, Germany, Iceland, Israel, Italy, Portugal, Hong Kong, Spain, The Netherlands, Chile.
Total Product Life CycleTPLC 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) Database510(K)s with Product Code = HGI
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