Posi-Stop Injection Needle — Class II medical device recall Z-0468-2025
Ongoing recall by Hobbs Medical, Inc., reported 2024-11-27, distributed nationwide. Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some
| Recall number | Z-0468-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hobbs Medical, Inc., Stafford Springs, CT, United States |
| Recall initiated | 2024-10-04 |
| Classified | 2024-11-15 |
| Reported by FDA | 2024-11-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 70 units |
| Lot numbers | H07-23-103, H07-23-104, H08-23-020, H09-23-111 |
| Model numbers | 4720 |
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0468-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.