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U.S. Department of Health and Human Services

Class 2 Device Recall Harmony

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 Class 2 Device Recall Harmonysee related information
Date Initiated by FirmApril 01, 2004
Date PostedAugust 14, 2004
Recall Status1 Terminated 3 on October 20, 2004
Recall NumberZ-1343-04
Recall Event ID 28977
510(K)NumberK033517 
Product Classification Spinal Vertebral Body Replacement Device - Product Code MQP
ProductHarmony MIS Life Instruments, Lumbar Spacer Systems manufactured by Spinal Concepts, Austin, Texas. Part numbers 2851-1-01, 2851-1-30, 2851-2-01, 2851-2-30, 2851-3-01, 2851-3-30, 2851-4-01, 2851-4-30, 2851-4-31, 2851-5-01, 2851-5-30, 2852-2, 2852-4, 2854-1, 2857-1, 2857-2, 2862-1, 2858-1, 2859-1, and 2861-5
Code Information 2851-1-01 lot number 18YH, 2851-1-30 lot number 18YJ, 2851-2-01 lot number 18YK, 2851-2-30 lot number 18YL, 2851-3-01 lot number 18YM, 2851-3-30 lot number 18YP, 2851-4-01, lot number 18YQ, 2851-4-30 lot number 18YR, 2851-4-31 lot number 18YS, 2851-5-01 lot number 18YT, 2851-5-30 lot number 18YW, 2852-2 lot number 18YT, 2852-4 lot number 18YT, 2854-1 lot number 18YX, 2857-1 lot number 18YZ, 2857-2 lot number 18ZA, 2862-1 lot number 18YY, 2858-1 lot number 18ZB, 2859-1 lot number 18ZC, and 2861-5 lot number 18ZD
Recalling Firm/
Manufacturer		 Spinal Concepts, Inc
5301 Riata Park Ct Bldg F
Austin TX 78727-3436
Manufacturer Reason
for Recall		Handle becomes loose after repeated use.
FDA Determined
Cause 2		Other
ActionTelephone calls were made 4/1/04 to consignees requesting inspection and return of the product.
Quantity in Commerce646 units
DistributionProduct was distributed domestically in the following states: TN, MI, KY, CA, CO, OH, KS, WA, TX, NY, AZ, PA, MA, UT, MO, IN, NV, OR, SD, IL, NJ, WI, OK, FL, GA, VA, NC, MD
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 = MQP
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