FDAClass IIAugust 24, 2016

Convenience Kits recall

Convenience Kits, MOHS "OPENING" PROCEDURE TRAY

Why was Convenience Kits 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.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Catalog No. MCVA0089-04 , LOT# 1010997

Product
Convenience Kits, MOHS "OPENING" PROCEDURE TRAY
Recalling firm
Avid Medical, Inc.
Quantity
240
Distribution
Recalled product was distributed to 2 states: Virginia and Massachusetts.
Recall date
August 24, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
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