AMD-Ritmed Transparent Dressing — Class II medical device recall Z-0727-2017
Terminated recall by Amd-Ritmed, Inc., reported 2016-12-14, distributed in MA, NY, TN, VA. The lot of transparent dressing was found to be contaminated (not sterile) based on FDA sampling and analysis.
| Recall number | Z-0727-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Amd-Ritmed, Inc., Tonawanda, NY, United States |
| Recall initiated | 2016-06-08 |
| Classified | 2016-12-08 |
| Reported by FDA | 2016-12-14 |
| Terminated | 2017-02-24 |
| Distributed | MA, NY, TN, VA |
| Reason classes | sterility |
| Lot numbers | 68408 |
Product
AMD-Ritmed Transparent Dressing - Window with label, 4 " x 4 3/4" (10 cm x 12 cm), Reorder No./Code A60044-W, Sterile -- 200 Dressings per case -- Made in China for AMD-Ritmed Inc. 1200 55th Ave., Lachine, QC H8T 3J8/295 Firetower Road, Tonawanda, NY 14150
Reason for recall
The lot of transparent dressing was found to be contaminated (not sterile) based on FDA sampling and analysis.
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-0727-2017. 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.