Windstone Medical Packaging recalls Monoject 0.9% Sodium Chloride 10mL syringes in specific kits from July 2019-July 2021 due to potential air reintroduction after expelling air. Affected kits include AMS-9041CP, AMS-9046CP-1, and others with listed lot numbers.
Monoject 0.9% Sodium Chloride Flush Syringe Manufactured by Cardinal Health and placed into kits. Potential for the plunger to draw back after air has been expelled and reintroduce air back into the syringe.
Windstone Medical Packaging recalls certain Monoject 0.9% Sodium Chloride 10mL syringes that came in specific medical kits from July 2019 to July 2021. The issue could cause air to be reintroduced into the syringe after expelling air, potentially affecting safe medical use.
The syringe's plunger may draw back after air is expelled, reintroducing air into the syringe. This could lead to air being injected into a patient's bloodstream during medical procedures, potentially causing complications.
Healthcare professionals using the recalled syringes in the specified medical kits are most at risk. Patients receiving injections with these syringes could face potential air reintroduction issues.
Check for the syringe model number 8881570121 inside Aligned Medical Solutions kits labeled AMS-9041CP, AMS-9046CP-1, AMS8939A, AMS9957A, or AMS12149. The syringes were manufactured between July 2019 and July 2021.
Look for the syringe model number 8881570121 inside the specified Aligned Medical Solutions kits.
Contact Windstone Medical Packaging for confirmation of the recalled syringe model and kit.
The syringe could allow air to be reintroduced after expelling air, potentially causing air to be injected into a patient's bloodstream during medical procedures.
The affected kits include AMS-9041CP, AMS-9046CP-1, AMS8939A, AMS9957A, and AMS12149 with specific lot numbers manufactured between July 2019 and July 2021.
Check for the syringe model number 8881570121 inside Aligned Medical Solutions kits labeled with the specific model numbers and lot numbers listed in the recall.
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-0119-2022 — Windstone Medical Packaging Windstone Medical Packaging Hello, I own a Windstone Medical Packaging that is covered by recall Z-0119-2022 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.
