PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge — Class II medical device recall Z-1946-2020
Terminated recall by Becton Dickinson & Company, reported 2020-05-20, distributed in AZ, CT, GA, IL, LA, MA, MI, MN…. Iincorrectly packaged without the required lidocaine as labeled
| Recall number | Z-1946-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2020-03-17 |
| Classified | 2020-05-08 |
| Reported by FDA | 2020-05-20 |
| Terminated | 2020-10-21 |
| Distributed | AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX |
| Quantity | 655 kits |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00801741139390 |
| Lot numbers | REDW0476 |
| Model numbers | ST018101D |
| Expiration dates | 2030-10-20 |
Product
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Reason for recall
Iincorrectly packaged without the required lidocaine as labeled
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-1946-2020. 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.