Churchill Medical Systems, A Vygon Company, Skin-Prep Wipes used in Convenience Kits
Friday, 03 June 2011 16:05
Recall -- Firm Press Release
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Churchill Medical Systems, A Vygon Company, Skin-Prep Wipes used in Convenience Kits
Contact:
Vygon Customer Service
1-800-473-5414
FOR IMMEDIATE RELEASE - June 1, 2011- Churchill Medical Systems, A Vygon Company, is initiating a nationwide recall of certain lots of 5 hospital-use convenience kits. These products contain Skin-Prep Wipes that were affected by an April 2011 recall initiated by Smith & Nephew due to the potential for bacterial contamination. The Skin-Prep Wipes were manufactured in the same facility as The Triad Group’s affected products. Testing was conducted by Smith & Nephew on product lots distributed and in quarantine and no contamination has been found to date. No injuries have been reported to Vygon as a result; however, Vygon is initiating this recall out of an abundance of caution as use of contaminated Skin-Prep Wipes could lead to life-threatening infections, especially in at risk populations, including immune suppressed and surgical patients. FDA has been apprised of this action.
The convenience kits were shipped to distributors and hospitals between September 3, 2010 and March 11, 2011. Consumers who have the following product lots of the 5 convenience kits named below should cease use and coordinate the return and replacement of product with Vygon immediately.
Product Code | Product Name | Lot Number |
AMS-7080CP | Dressing Change Kit | 10J29 |
10J55 | ||
11A18 | ||
11A47 | ||
11B06 | ||
AMS-8316CP-1 | Central Line Dressing Kit | 10I60 |
10K42 | ||
10F87 | ||
AMS-8431CP | PICC Insertion Tray | 10H30 |
AMS-9189CP-1 | Dressing Change Kit | 1006150 |
|
| 1006149 |
|
| 1008143 |
AMS-9189CP | Dressing Change Kit | 1003527 |
Consumers with questions should contact Vygon’s Customer Service Department Monday through Friday from 8:30 am and 6:00 pm Eastern Time at 1-800-473-5414.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
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