FDA Device recall Z-1925-2019
First Step Draco Pad, Product Number EP-4D
- FDA Device
- Class II
- terminated
- Published 2019-07-10
On 2019-07-10 the FDA classified a Class II recall of First Step Draco Pad, Product Number EP-4D by Madison Polymeric Engineering, citing this product has been contaminated with Stenotrophomonas lactiubi.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1925-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-05-08 |
| Published | 2019-07-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Madison Polymeric Engineering |
| Distribution | AZ, CA, FL, IA, IL, IN, MA, MD, MO, PA, TN, TX, WA |
Product
First Step Draco Pad, Product Number EP-4D
Reason
This product has been contaminated with Stenotrophomonas lactiubi.
Identifiers
| code_info | Lot Numbers EX20191221X EX20191226X EX20191227X EX20191228X |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1925-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.