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U.S. Department of Health and Human Services

Class 2 Device Recall Safe Connect

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  Class 2 Device Recall Safe Connect see related information
Date Initiated by Firm May 19, 2010
Date Posted August 13, 2010
Recall Status1 Terminated 3 on November 29, 2010
Recall Number Z-2223-2010
Recall Event ID 55804
510(K)Number K971968  
Product Classification Cable, transducer and electrode, patient (including connector) - Product Code DSA
Product Disposable Surgical Cable, Product Code: FL-601-97 (100), Single use, Rx Only, Remington Medical, Inc., 6830 Meadowridge Court, Alpharetta, GA 30005

Usage: Temporary pacing of open hearts: used with External Pacing Generators (EPGs).
Code Information Lot number: 100701
Recalling Firm/
Remington Medical Inc.
6830 Meadowridge Ct.
Alpharetta GA 30005
For Additional Information Contact Lynne Buchanan-Kopp
Manufacturer Reason
for Recall
The Safe Connect component may separate from the cable, causing the cable to become unplugged from the EPG.
FDA Determined
Cause 2
Process design
Action Consignees were notified on/about 05/19/2010. They were instructed to examine their inventory and quarantine product subject to the recall. If they distributed the product, they were advised to identify their customers and notify them of the recall (via the recall letter). A Return Authorization was provided. More information can be obtained by calling 770.888.8520.
Quantity in Commerce 1488 units
Distribution AZ, CA, CO, CT, DE, FL, GA, IL, IN, LA, MD, MI, MO, MS, NC, NM, NY, OH, OK, OR, PA, SC, TX, TN, TX, VA, WA, WI and Canada.
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 = DSA and Original Applicant = REMINGTON MEDICAL, INC.