CarePoint 60 mL Syringe Without Needle — Class II medical device recall Z-0478-2023
Completed recall by Allison Medical, Inc., reported 2022-12-21, distributed in FL, IA, LA, MS, PR. Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effec
| Recall number | Z-0478-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Allison Medical, Inc., Littleton, CO, United States |
| Recall initiated | 2020-09-03 |
| Classified | 2022-12-13 |
| Reported by FDA | 2022-12-21 |
| Distributed | FL, IA, LA, MS, PR |
| Countries outside the US | BB |
| Quantity | 2,004 boxes |
| Reason classes | potency |
| UPC / GTIN / UDI-DI | 00786227756059 |
| Lot numbers | 04-7560, 80522 |
| Model numbers | 04-7560 |
Product
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Reason for recall
Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown.
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-0478-2023. 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.