FDA Device recall Z-2007-2026
Medical Action Industries Inc
- FDA Device
- Class I
- ongoing
- Published 2026-05-13
On 2026-05-13 the FDA classified a Class I recall of Medical Action Industries Inc by Medical Action Industries 306, citing convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold".
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2007-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-03-17 |
| Published | 2026-05-13 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medical Action Industries 306 |
| Distribution | AZ |
Product
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Reason
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
Identifiers
| code_info | UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
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-2007-2026%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.