FDA Device recall Z-0147-2022
Kit: Central Line Dres Change 20/Cs
- FDA Device
- Class II
- terminated
- Published 2021-10-27
On 2021-10-27 the FDA classified a Class II recall of Kit: Central Line Dres Change 20/Cs by Medical Action Industries 306, citing the ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0147-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-09-08 |
| Published | 2021-10-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medical Action Industries 306 |
| Distribution | MI |
Product
Kit: Central Line Dres Change 20/Cs
Reason
The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.
Identifiers
| code_info | Product Code: 59815B, Batch 0000285665; Kit expiration date 03/31/2024 UDI: 20809160170523 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Medical Action Industries 306
- Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot Number: 333606 UDI-DI: 208…
FDA Device · Class III · 2026-10-14 · Medical Action Industries 306 - Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451
FDA Device · Class II · 2026-09-23 · Medical Action Industries 306 - Kit: Single Shot Epidural 20/Cs, REF: 59553
FDA Device · Class I · 2026-09-16 · Medical Action Industries 306 - Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
FDA Device · Class I · 2026-09-16 · Medical Action Industries 306 - Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
FDA Device · Class II · 2026-08-12 · Medical Action Industries 306
All Medical Action Industries 306 recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0147-2022%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.