← FDA ENFORCEMENT
Z-1727-2026Class I

Medline Industries, LP

Recalling firm
Medline Industries, LP
Product type
Device
Status
Ongoing
Report date
2026-04-15
Distribution
Worldwide distribution: US (nationwide) including Puerto Rico (PR) and OUS (foreign) to countries of: Canada (CA), Netherlands (NL), Australia (AU), Korea, Republic of (KR), Sri Lanka (LK), Pakistan (PK), Japan (JP), United Arab Emirates (AE), Singapore (SG) and Slovakia (SK).
Firm state
IL
Product quantity
966 kits
Initiated by
Voluntary: Firm initiated
Reason for recall

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Product description

Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. DELIVERY PACK, Medline SKU # DYNJ42892F; 2. DELIVERY PACK, Medline SKU # DYNJ42892G.

Code / lot info

Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25GMD696; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25EMJ573; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25DMC646; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25BMD630; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24LMA523; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24KMA084; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24JME306; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24FME624; Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24EMF099; Medline SKU # DYNJ42892G, UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 26BMH149; Medline SKU # DYNJ42892G, UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 26AMD029; Medline SKU # DYNJ42892G, UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 25KMA060; Medline SKU # DYNJ42892G, UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 25IMA514.

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.