FDA Recall Terminated

Totalis, RIGID and Totalis"I Flex ENDO KIT, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.

Recall: Z-0406-2017 · Initiated October 13, 2016

Recall

Recall Number
Z-0406-2017
Event Number
75492
Firm
C.R. Bard, Inc.
FEI Number
1018233
Product Code
FAD
Status
Terminated
Root Cause
Labeling Change Control
Initiated
October 13, 2016
Terminated
February 10, 2022
Address
8195 Industrial Blvd NE, Covington, GA, 30014-1497

Description

Totalis, RIGID and Totalis"I Flex ENDO KIT, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.

Reason

Labeling: Statement was added to the Warnings/Precautions section requesting end users to consider the presence of a knot if significant resistance is encountered during attempts at removal.

Action

Bard Medical sent an Urgent: Medical Device Communication Letter dated October 13, 2016, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Action required: Examine your inventory and identify any product subject to this notification. If you have any remaining inventory, include a copy of this communication with the unit(s) for future use. If you may have further distributed or transferred this product, please identify the respective organizations and notify them at once of this communication. Your notification to these organizations may be enhanced by including a copy of this product communication letter. This notification should be carried out to the user level. This product notification is being made with the knowledge of the Food and Drug administration. We appreciate your cooperation and assistance in dealing with this matter and sincerely apologize for any inconvenience that may result from this action. For further questions, please call (770) 784-6220.

Distribution

U.S. Nationwide.

Quantity

75,089 units