Kit: Midline Insertion DA — Class I medical device recall Z-1556-2021
Terminated recall by Medical Action Industries, Inc. 306, reported 2021-05-19, distributed nationwide. Medical convenience kits are being recalled due to a potential breach in the package integrity of a component,
| Recall number | Z-1556-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Action Industries, Inc. 306, Arden, NC, United States |
| Recall initiated | 2021-04-09 |
| Classified | 2021-05-12 |
| Reported by FDA | 2021-05-19 |
| Terminated | 2023-10-03 |
| Distributed | Nationwide (US) |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 20809160284053 |
| Lot numbers | 0000281502 |
| Model numbers | 77981B |
| Expiration dates | 2021-07-09, 2021-11-13, 2022-04-08 |
Product
Kit: Midline Insertion DA. MAI Kit Part Number: 77981B
Reason for recall
Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
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-1556-2021. 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.