FDA Recall Terminated

AVID Medical QA Pack AV10654-10

Recall: Z-0581-2018 · Initiated July 3, 2017

Recall

Recall Number
Z-0581-2018
Event Number
79135
Firm
Avid Medical, Inc.
FEI Number
1047429
Product Code
LRO
Status
Terminated
Root Cause
Process control
Initiated
July 3, 2017
Terminated
April 17, 2018
Address
9000 Westmont Dr, Toano, VA, 23168-9351

Description

AVID Medical QA Pack AV10654-10

Reason

The swab stick collection device provided in a convenience kit expires prior to the kit expiration date.

Action

Avid Medical began shipping this product on 05/23/2017. Immediately examine your inventory and quarantine all product subject to this correction. In addition, if you may have further distributed this product, please identify your customers and notify them at once of this product correction. Your notification to your customers may be enhanced by including a copy of this Urgent Medical Device Correction notice. Please complete the attached Correction Response Form as soon as possible. Attached is a label template for use in the generation of an appropriate warning label for application on all AV10654-10 inventory of impacted lot 1235229. This label should be applied to each affected convenience kit and product case in a prominently visible location to end-users. The location chosen should not cover any other critical product information found on existing product labeling. If you prefer to have labels printed for your facility, please send quantity and end-user location information request to [email protected]. Replacement component swab stick collection systems are available upon request. This correction will be executed with oversight of the associated account sales rep. Please complete and return the enclosed response form as soon as possible.

Distribution

Seventeen sites located in 13 states: FL, IN, KS, KY, MA, OK, NC, NE, NY, OH, PA, VA, and TX.

Quantity

330