Official recall record
Cardinal Health Monoject, 6ML Enteral Syringe (purple) Low Dose (LDT) - For Use with ENFit Connection System, REF 406SE
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-12-28
- Country of alert
- United States
- Alert level
- Class I
- Alert type
- recall
- Barcode (EAN/GTIN)
- 26971564466220
- Brand on record
- Cardinal Health 200, LLC
- Product category
- Medical Device
What the authority reported
The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility issues with certain syringe enteral feeding pumps. As a result, Cardinal Health recommends that they not be used with enteral syringe feeding pumps.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2026-08-19 · US FDA — Medical Devices
Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 - 2026-08-18 · US FDA — Medical Devices
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catal - 2026-08-18 · US FDA — Medical Devices
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAVH , Catal
All 31 official recall notices naming Cardinal Health 200, LLC on this site →
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