MAMMOGRAPHY — Class II medical device recall Z-2592-2016
Terminated recall by Avid Medical, Inc., reported 2016-08-24, distributed in MA, VA. Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included
| Recall number | Z-2592-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Avid Medical, Inc., Toano, VA, United States |
| Recall initiated | 2015-10-05 |
| Classified | 2016-08-18 |
| Reported by FDA | 2016-08-24 |
| Terminated | 2017-01-10 |
| Distributed | MA, VA |
| Quantity | 200 |
| Reason classes | labeling |
| Lot numbers | 1021706 |
| Model numbers | LGHM022-02 |
Product
MAMMOGRAPHY
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2592-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.