Recall Z-2590-2016— Avid Medical, Inc.
Class II · Terminated
Class II FDA medical device recall by Avid Medical, Inc., initiated 2015-10-05, terminated 2017-01-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Convenience Kits, MOHS "OPENING" PROCEDURE TRAY. Reason: Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex..
- Recalling firm
- Avid Medical, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-10-05
- Terminated
- 2017-01-10
- Firm location
- Toano, VA, United States
Product description
Convenience Kits, MOHS "OPENING" PROCEDURE TRAY
Reason for recall
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
Data sourced from openFDA. This site is unofficial and independent of the FDA.