Cardinal Health recalls 35mL purple enteral syringes with ENFit connection that may not work safely with enteral feeding pumps. Affected units have specific lot numbers and require immediate action to prevent feeding pump malfunctions.
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.
Cardinal Health is recalling 35mL purple enteral syringes that may not work safely with certain enteral feeding pumps. Using these syringes with feeding pumps could cause improper feeding and potential safety risks.
The syringes have recognition and compatibility issues with certain enteral feeding pumps. This means they might not work properly, leading to improper feeding and potential safety risks.
People using enteral feeding pumps with these specific syringes are affected. Those who have the syringes with the listed lot numbers are most at risk.
Check for purple 35mL syringes labeled 'For Use with ENFit Connection System' with the lot numbers 230501, 230601, or 230602. The product has a unique identifier (UDI/DI) starting with 26971564466244.
Look for lot numbers 230501, 230601, or 230602 on the syringe packaging.
Do not use these syringes with enteral feeding pumps as they may not work safely.
The syringes have recognition and compatibility issues with certain enteral feeding pumps, which could lead to improper feeding and safety risks.
Lot numbers 230501, 230601, and 230602.
Check for purple 35mL syringes with the ENFit connection system and lot numbers 230501, 230601, or 230602.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0849-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0849-2024 from Cardinal Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
