Allison Medical, Inc. recalls CarePoint 60 mL Syringe Without Needle, REF: 04-7560
- Recall date
- September 3, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0478-2023
- FDA classification
- Class II
- Brand / firm
- Allison Medical, Inc.
- Sold / distributed
- US: IA, LA, MS, FL, PR; OUS: BARBADOS
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
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