# FDA recall Z-0478-2023

> **Allison Medical, Inc.** · Class II · device recall initiated 2020-09-03.

## 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.

## Distribution

US: IA, LA, MS, FL, PR; OUS: BARBADOS

## Key facts

- **Recall number:** Z-0478-2023
- **Recalling firm:** Allison Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2020-09-03
- **Report date:** 2022-12-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Littleton, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0478-2023

## Citation

> AI Analytics. FDA recall Z-0478-2023. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-0478-2023. Source: US FDA. Licensed CC0.

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