CarePoint 60 mL Syringe (Allison Medical) - Plunger substance concern (2020)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Brand
Allison Medical, Inc.
Lot Codes / Batch Numbers
UDI-DI: 00786227756059, REF/Lot: 04-7560/ 80522
Products Sold
UDI-DI: 00786227756059, REF/Lot: 04-7560/ 80522
Allison Medical, Inc. is recalling CarePoint 60 mL Syringe Without Needle, REF: 04-7560 due to 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 unkn. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
FL, IA, LA, MS, PR
Page updated: Jan 10, 2026