FDA Device recall Z-0478-2023
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
- FDA Device
- Class II
- completed
- Published 2022-12-21
On 2022-12-21 the FDA classified a Class II recall of CarePoint 60 mL Syringe Without Needle, REF: 04-7560 by Allison Medical, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0478-2023 |
| Classification | Class II |
| Status | completed |
| Initiated | 2020-09-03 |
| Published | 2022-12-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Allison Medical |
| Distribution | FL, IA, LA, MS, PR |
Product
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Reason
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.
Identifiers
| code_info | UDI-DI: 00786227756059, REF/Lot: 04-7560/ 80522 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0478-2023%22
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