Class II

Medical Device Recall: Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716

Hobbs Medical, Inc. · October 4, 2024

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.

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.

States Affected

NATIONWIDE

Quantity Affected

5 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0471-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Hobbs Medical, Inc. Medical Device Recall: Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716 | SafeCheck