PlainRecalls
FDA Devices Moderate Class II Terminated

Convenience Kits, MOHS "OPENING" PROCEDURE TRAY

Reported: August 24, 2016 Initiated: October 5, 2015 #Z-2590-2016

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.

Details

Recalling Firm
Avid Medical, Inc.
Units Affected
240
Distribution
Recalled product was distributed to 2 states: Virginia and Massachusetts.
Location
Toano, VA

Frequently Asked Questions

What product was recalled?
Convenience Kits, MOHS "OPENING" PROCEDURE TRAY. Recalled by Avid Medical, Inc.. Units affected: 240.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 24, 2016. Severity: Moderate. Recall number: Z-2590-2016.