|
Class 2 Device Recall Zimmer Hemovac Wound Drainage Device Infection Control Kits |
|
Date Initiated by Firm |
January 31, 2008 |
Date Posted |
April 09, 2008 |
Recall Status1 |
Terminated 3 on November 12, 2009 |
Recall Number |
Z-1457-2008 |
Recall Event ID |
46792 |
Product Classification |
Wound Drainage Device Infection Control Kits - Product Code GCY
|
Product |
Zimmer Hemovac Wound Drainage Device Infection Control Kits, Catalog Number; 47-2550-003-10; 400 ml evacuators and 450 ml collection bags, 3/16 in. (15 FR.) O.D. middle perforated PVC drains with trocars, evaluator tubing and connectors, soft, contains 10, non-sterile, latex free, Zimmer, Dover, Ohio |
Code Information |
Lot Numbers; 32331100, 32531400, 32944300, 33078800, 33208400, 33342100, 60006805, 60045252, 60088425, 60118920, 60174047, 60215672, 60269221, 60321524, 60385874, 60540737, 60564969, 60607918 and 60629972. |
Recalling Firm/ Manufacturer |
Zimmer Inc. 345 E Main St Warsaw IN 46580-2746
|
For Additional Information Contact |
330-365-3793
|
Manufacturer Reason for Recall |
Leakage; The kits may disassemble at the fluid collection port, which would present a risk of exposure to blood borne pathogens to health care providers should it occur during use.
|
FDA Determined Cause 2 |
Process control |
Action |
Consignees were notified via Urgent Infection Control Recall letter dated 1/31/08 to examine their inventory and return the recalled lots. Custom kit packers were instructed in the same letter to recall these products/lots from their own customers. |
Quantity in Commerce |
34,354 (Recalls Z-1448/1458-2008) |
Distribution |
Worldwide-USA, Australia, Canada, Colombia, Denmark, Dubai, Italy, Japan, Mexico and Singapore. |
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.
|
|
|
|