Windstone Medical Packaging recalls Custom Convenience Kits Pre Op Kit - NS (Part AMS14994A) due to potential backflow of medication between IV containers. Affected units include specific lot numbers.
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
Windstone Medical Packaging is recalling Custom Convenience Kits Pre Op Kit - NS (Part Number AMS14994A) because it can cause medication to flow backward between IV containers, potentially causing contamination. This risk is serious enough to require immediate action to prevent harm.
The kit can allow medication to flow backward from secondary IV containers into primary containers or other connections. This backflow could cause contamination or incorrect dosing of medication during IV treatments.
Patients receiving IV treatments using this specific kit are most at risk. Healthcare providers using the recalled product for pre-op procedures should check their inventory.
Check for the part number AMS14994A on the kit. Affected units include lot numbers 224792, 228566, 230105, 230853, and 234209.
Immediately stop using the recalled Custom Convenience Kits Pre Op Kit - NS (Part Number AMS14994A) if you have it.
The part number is AMS14994A.
Lot numbers 224792, 228566, 230105, 230853, and 234209 are affected.
Check the part number on the kit and compare it to AMS14994A. Also, verify the lot number against the listed numbers.
We’ve drafted a message you can send Windstone Medical Packaging to request your refund or repair — edit it as you like.
Subject: Recall Z-1921-2026 — Windstone Medical Packaging Windstone Medical Packaging Hello, I own a Windstone Medical Packaging that is covered by recall Z-1921-2026 from Windstone Medical Packaging. 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.
