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Completed

CarePoint 60 mL Syringe Without Needle, REF: 04-7560

FDA Recall Z-0478-2023 · Posted 2022-12-13

Recalling FirmAllison Medical, Inc.
Recall StatusCompleted
Product CodeFMF
Date Initiated2020-09-03
Product Quantity2,004 Boxes

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.

Firm Action

On 9/3/20, and later on 3/2/21, recall notices were emailed to customers who were informed to stop using and destroy or return affected devices to the recalling firm. Customers with additional questions could contact the recalling firm at 801-510-8733.

Root Cause

Nonconforming Material/Component

Distribution Pattern

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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