Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection solutions would not flow as intended through...

Date: October 4, 2024
Company: Hobbs Medical, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Hobbs Medical, Inc. directly.

Affected Products

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

Quantity: 45 units

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Hobbs Medical, Inc.

Hobbs Medical, Inc. has 73 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report