FDA Device recall Z-0751-2023
Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
- FDA Device
- Class II
- terminated
- Published 2022-12-28
On 2022-12-28 the FDA classified a Class II recall of Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit by Medical Action Industries 306, citing XXX.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0751-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-11-04 |
| Published | 2022-12-28 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medical Action Industries 306 |
| Distribution | US |
Product
Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
Reason
XXX
Identifiers
| code_info | UDI/DI 10809160156681, Lot Numbers: 297223, 297418 |
|---|
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-0751-2023%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.