Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702

FDA Recall #Z-0469-2025 — Class II — October 4, 2024

Recall #Z-0469-2025 Date: October 4, 2024 Classification: Class II Status: Ongoing

Product Description

Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702

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.

Recalling Firm

Hobbs Medical, Inc. — Stafford Springs, CT

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

45 units

Distribution

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.

Code Information

Catalog Number: 4702; UDI-DI: M84947020; Lot Numbers: H08-23-263, H01-24-114.

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated