Medela recalls ENFit ExSet Strl 60 2.0ml PV 1ct EN due to incompatible connectors that may cause delays in feeding or medication delivery. Affected units have model ENF060182LD or 101033086.
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.
Medela is recalling its ENFit ExSet Strl 60 2.0ml PV 1ct EN product because it may have incorrect connectors that don't attach properly. This could cause delays in delivering enteral nutrition or oral medication to patients.
The connectors may not attach correctly to ENFit connections, leading to delays in delivering nutrition or medication. This is a compatibility issue that does not cause injury but may disrupt treatment schedules.
Parents or caregivers using this feeding system for infants or patients who require enteral nutrition are most at risk. The product is intended for medical use in healthcare settings.
Check for model numbers ENF060182LD or 101033086 on the product packaging. The product was manufactured on January 16, 2026, and expires January 16, 2029.
Look for model numbers ENF060182LD or 101033086 on the packaging or product label.
The product may have incorrect connectors that don't attach properly to ENFit connections, which could cause delays in delivering enteral nutrition or oral medication.
Check for model numbers ENF060182LD or 101033086 on the packaging or product label. The product was manufactured on January 16, 2026, and expires January 16, 2029.
The recall does not specify a remedy, so contact Medela directly for guidance on next steps.
We’ve drafted a message you can send Medela to request your refund or repair — edit it as you like.
Subject: Recall Z-2645-2026 — Medela Medela Hello, I own a Medela that is covered by recall Z-2645-2026 from Medela. 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.
