Allison Medical, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0478-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 3, 2020

Date Posted: December 21, 2022

Recall Number: Z-0478-2023

Event ID: 91092

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.

Status: Completed

Product Quantity: 2,004 Boxes

Code Information:

UDI-DI: 00786227756059, REF/Lot: 04-7560/ 80522

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated