FDA Device recall Z-0470-2025
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
- FDA Device
- Class II
- ongoing
- Published 2024-11-27
On 2024-11-27 the FDA classified a Class II recall of Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706 by Hobbs Medical, citing 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 inn….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0470-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-10-04 |
| Published | 2024-11-27 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Hobbs Medical |
| Distribution | US |
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
Reason
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.
Identifiers
| code_info | Catalog Number: 4706; UDI-DI: M84947060; Lot Number: SD09-23-089. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0470-2025%22
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