FDA Medical Device Recalls (openFDA)
Avid Medical, Inc.: Convenience Kits, MOHS "OPENING" PROCEDURE TRAY
- Recall number
- Z-2590-2016
- Recalling firm
- Avid Medical, Inc.
- Product
- Convenience Kits, MOHS "OPENING" PROCEDURE TRAY
- Status
- Terminated
- Initiated
- 2015-10-05
- Posted
- 2016-08-18
- Terminated
- 2017-01-10
- 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.
- Root cause
- Employee error
- Action
- Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 cm) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
- Quantity
- 240
- Distribution
- Recalled product was distributed to 2 states: Virginia and Massachusetts.
- Lot, serial or model codes
- Catalog No. MCVA0089-04 , LOT# 1027144
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LRO
- Firm FEI
- 1047429
- Firm city
- Toano
- Firm state
- VA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28