Hobbs Medical, Inc.: Device Recall
Recall #Z-0468-2025 · 10/04/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0468-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Hobbs Medical, Inc.
- Status
- Ongoing
- Date Initiated
- 10/04/2024
- Location
- Stafford Springs, CT, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 70 units
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.
Product Description
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
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.
Other Recalls by Hobbs Medical, Inc.
- Class II: Risk 10/04/2024
- Class II: Risk 10/04/2024
- Class II: Risk 10/04/2024
- Class II: Risk 10/04/2024
- Class II: Risk 10/04/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.