Hobbs Medical, Inc.: Medical Device Recall in 2024 - (Recall #: Z-0475-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722

Product Classification:

Class II

Date Initiated: October 4, 2024

Date Posted: November 27, 2024

Recall Number: Z-0475-2025

Event ID: 95577

Reason for Recall:

Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.

Status: Ongoing

Product Quantity: 198 units

Code Information:

Catalog Number: 4722; UDI-DI: M84947220; Lot Numbers: H08-23-265, H09-23-113, H10-23-223, H11-23-058.

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated