HUMAN MED AG: Medical Device Recall in 2025 - (Recall #: Z-1251-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use.

Product Classification:

Class II

Date Initiated: October 18, 2024

Date Posted: March 12, 2025

Recall Number: Z-1251-2025

Event ID: 96137

Reason for Recall:

The cannula tubes do not comply with the specification. The water jet emerging from the nozzle of the nonconforming cannulas may emerge as a spot jet rather than a fan-shaped spray jet.

Status: Ongoing

Product Quantity: 775 devices

Code Information:

Lot number 24-20198, UDI (01)04260170881014(11)240611(17)270611(10)24-20198; and Lot number 23-19612, UDI (01)04260170881014(11)240109(17)270109(10)23-19612.

Distribution Pattern:

US Nationwide distribution in the state of FL.

Voluntary or Mandated:

Voluntary: Firm initiated