Home › DELTA MED SPA › Deltaven Fast Flash
Deltaven Fast Flash
DELTA MED SPA · Model 3831473 · UDI-DI 08032248383142
FOZ
Prescription
10
510(k) clearances
48,998
Adverse events (141 deaths)
394
Recalls
198
Facilities
Description
Safety IV catheter in PUR with closed system, dual entry with two needleless valves
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-11 | ARROW INTERNATIONAL, LLC | Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured |
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
| 2025-05-21 | Becton Dickinson Infusion Therapy Systems, Inc. | Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.