FDAClass IIDecember 21, 2022

CarePoint recall

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

Why was CarePoint 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.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Recalling firm
Allison Medical, Inc.
Quantity
2,004 Boxes
Distribution
US: IA, LA, MS, FL, PR; OUS: BARBADOS
Recall date
December 21, 2022
Classification
Class II
Status
Completed
Agency
FDA (device)
Open FDA enforcement record Latest recalls