FDA Device recall Z-2592-2016
MAMMOGRAPHY
- FDA Device
- Class II
- terminated
- Published 2016-08-24
On 2016-08-24 the FDA classified a Class II recall of MAMMOGRAPHY by Avid Medical, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2592-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-10-05 |
| Published | 2016-08-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Avid Medical |
| Distribution | MA, VA |
Product
MAMMOGRAPHY
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.
Identifiers
| code_info | Catalog No. LGHM022-02 , LOT# 1021706 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2592-2016%22
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