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U.S. Department of Health and Human Services

Class 2 Device Recall MediChoice Rayon Tipped OB/GYN Applicator

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 Class 2 Recall
MediChoice Rayon Tipped OB/GYN Applicator
see related information
Date Posted May 01, 2013
Recall Status1 Open
Recall Number Z-1192-2013
Recall Event ID 64919
Product Classification Applicator, Absorbent Tipped, Non-Sterile - Product Code KXF
Product MediChoice® Rayon Tipped OB/GYN Applicator, 8 inch, Plastic Shaft, Non-Sterile, Item Numbers WOD5001 and WOD5002. Product Usage: Usage: An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.
Code Information Item # Lot# WOD5001 1206DG13A WOD5001 1206DG13B WOD5001 1207DG13A WOD5001 1208DG13A WOD5001 1209DG13A WOD5001 1210DG13A/B WOD5001 1211DG13A WOD5001 1212DG13A WOD5001 1301DG13A WOD5001 1303DG13A WOD5002 1206DG14A WOD5002 1208DG14A WOD5002 1209DG14A WOD5002 1211DG14A Expiration Dates: 2017-05, 2017-06, 2017-06, 2017-07, 2017-08, 2017-09, 2017-10, 2017-11, 2018-02.
Recalling Firm/
Manufacturer
Owens & Minor Distribution, Inc.
9120 Lockwood Blvd
Mechanicsville, Virginia 23116-2015
Manufacturer Reason
for Recall
Owens & Minor Distribution, Inc. is conducting a market withdrawal of MediChoice Applicator OB-GYN 8 inch product that does not meet our quality standards because the rayon may loosen or unravel from the applicator during use.
FDA Determined
Cause 2
PRODUCTION CONTROLS: Process Control
Action Owens&Minor sent an Urgent: Medical Device Recall letter to the first set of customers on March 26, 2013 and to their second set of customers on April 9, 2013. The letter identified the affect product, problem and actions to be taken. Customers were instructed to examine their inventory and quarantine all affected products, contact service representative to discuss whether affected products should be returned or destroyed, and complete and return the Recall Reply Form. For questions call 804-723-7417.
Quantity in Commerce 4298.5 cases
Distribution US Nationwide Distribution.
Total Product Life Cycle TPLC Device Report

 
1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
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