FDA Device recall Z-1554-2021
Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420
- FDA Device
- Class I
- terminated
- Published 2021-05-19
On 2021-05-19 the FDA classified a Class I recall of Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420 by Medical Action Industries 306, citing medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1554-2021 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2021-04-09 |
| Published | 2021-05-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medical Action Industries 306 |
| Distribution | US |
Product
Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420
Reason
Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Identifiers
| code_info | Kit Number: 79420; UDI (GTIN): 20809160247775; Lot Number: 0000276767 (Expiration Date: 01/31/2022), 0000278361 (Expira…Kit Number: 79420; UDI (GTIN): 20809160247775; Lot Number: 0000276767 (Expiration Date: 01/31/2022), 0000278361 (Expiration Date: 05/31/2022), and 0000281458 (Expiration Date: 08/31/2022) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1554-2021%22
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