PlainRecalls
FDA Devices Moderate Class II Ongoing

Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723

Reported: November 27, 2024 Initiated: October 4, 2024 #Z-0476-2025

Product Description

Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723

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.

Details

Recalling Firm
Hobbs Medical, Inc.
Units Affected
10 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.
Location
Stafford Springs, CT

Frequently Asked Questions

What product was recalled?
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723. Recalled by Hobbs Medical, Inc.. Units affected: 10 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 27, 2024. Severity: Moderate. Recall number: Z-0476-2025.