Data Foundry

Medical device recalls 2026

Medline medical convenience kits — Class I medical device recall Z-1721-2026

Ongoing recall by Medline Industries, LP, reported 2026-04-15, distributed nationwide. Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotatin

Recall numberZ-1721-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-02-27
Classified2026-04-07
Reported by FDA2026-04-15
DistributedNationwide (US)
Countries outside the USAE, AU, CA, JP, KR, LK, NL, PK, SG, SK
Quantity594 kits
UPC / GTIN / UDI-DI10195327054519, 10195327686888, 10195327692469, 10198459205552, 10889942814619, 40195327054510, 40195327686889, 40195327692460, 40198459205553, 40889942814610
Lot numbers24EBG342, 24EMD869, 24GBO586, 24JMC622, 24LLA039, 25AMH487, 25EBR802, 25HBU295

Product

Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. HEAD AND NECK CDS-LF, Medline SKU # CDS780138K; 2. HEART CATH PACK-LF, Medline SKU # DYNJ36478B; 3. HEART CATH PACK-LF, Medline SKU # DYNJ36478B; 4. HEART CATH PACK-LF, Medline SKU # DYNJ36478B; 5. THYROIDECTOMY, Medline SKU # DYNJ910458; 6. LH 3 PORT W/O WASTEBAG, Medline SKU # VASC1081C; 7. LHK, Medline SKU # VASC1510; 8. LHK, Medline SKU # VASC1510.

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1721-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.