Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Spectrum Designs Medical Anatomical Chin Implant

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 2 Device Recall Spectrum Designs Medical Anatomical Chin Implantsee related information
Date Initiated by FirmJuly 24, 2007
Create DateJune 25, 2015
Recall Status1 Terminated 3 on July 29, 2011
Recall NumberZ-1265-2007
Recall Event ID 44735
510(K)NumberK944164 
Product Classification Anatomical Chin Implant - Product Code LZK
ProductSpectrum Designs Medical Anatomical Chin Implant; Catalog Number 250-134S; Lot # 31140; Serial Numbers BAHO45 through BAH144
Code Information Catalog Number 250-134S; Lot # 31140; Serial Numbers BAHO45 through BAH144
Recalling Firm/
Manufacturer		 Spectrum Designs Inc
6387 Rose Ln Ste B
Carpinteria CA 93013-2937
For Additional Information ContactJim Dishman
805-684-7678
Manufacturer Reason
for Recall		Mispackaging/Mislabeing: a portion of the lot may be labeled as containing nasal implants
FDA Determined
Cause 2		Other
ActionThe firm initiated the recall on 07/24/2007 by contacting the customer (distributor) who filed the original complaint of mislabeling by email. The firm followed-up by sending recall letters (dated July 24, 2007) via FedEx or certified mail with signature confirmation to the one other direct account who received the recalled product on 08/03/2007. Customers were instructed to check their inventory for mislabeled products and call Spectrum at (800)239-6399 to report the number of this product being returned. They were given an address for product return. The firm indicated they will examine returned products, and scrap after examination.
Quantity in Commerce100
DistributionNationwide: California and China
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 = LZK
-
-