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U.S. Department of Health and Human Services

Class 3 Device Recall FormPutty Bone Void Filler 10cc

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 Class 3 Device Recall FormPutty Bone Void Filler 10ccsee related information
Date Initiated by FirmJuly 11, 2008
Date PostedSeptember 18, 2008
Recall Status1 Terminated 3 on September 20, 2011
Recall NumberZ-2375-2008
Recall Event ID 49018
510(K)NumberK053228 
Product Classification Calcium Compound Bone Void Filler - Product Code MQV
ProductFormPutty Bone Void Filler 10cc The product is sealed in a foil pouch and then placed in a box following sterilization. Part # 50-07-0100 Is a flowable resorbable porous bone void filler composed of beta tricalcium phosphate and other calcium phosphates.
Code Information Lot # A08F01E Exp Date 2010-06
FEI Number 3002498892
Recalling Firm/
Manufacturer		 Theken Spine LLC
1800 Triplett Blvd
Akron OH 44306-3311
For Additional Information ContactSuzanne Wojcik
330-475-8643
Manufacturer Reason
for Recall		The patient label inside the package has an expiration date of 2008-06 when the actual expiration date is 2010-06.
FDA Determined
Cause 2		Labeling mix-ups
ActionIn a letter dated July 11, 2008, the firm asked their customers to check their inventory for the suspect product. If found they are to return the product for credit or replacement. The firms asks customers to contact them if any units were used for surgery and they will send the correct patient labels. If additional information is needed, customers are to contact Theken Spine Regulatory Affairs or the Quality Department.
Quantity in Commerce33 syringes
DistributionNationwide Distribution --- including states of FL, OH, TX, and UT.
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 = MQV
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