Becton Dickinson recalls Alaris Pump Infusion Sets with specific model codes due to potential medication delivery errors. Affected units may cause unintended medication delivery or faster-than-expected drug flow.
An incomplete occlusion can be caused by a variation in the wall thickness of the pumping segment of the affected infusion sets used with the. The issue has the potential to lead to unintended delivery of medication when the pump module is not in running status or can result in faster than expected drug delivery flow when the pump is infusing.
Becton Dickinson is recalling certain Alaris Pump Infusion Sets that could cause unintended medication delivery or faster-than-expected drug flow when the pump is not running or infusing. This risk affects patients receiving intravenous treatments.
The pumping segment of the affected infusion sets has varying wall thickness, which can cause incomplete occlusion. This may lead to unintended medication delivery when the pump is not running or faster-than-expected drug delivery when the pump is infusing.
Patients using the recalled infusion sets for intravenous medication administration are most at risk. Healthcare providers who use these sets with patients should check if their equipment is affected.
Check for model codes listed in the recall: 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930, and others. The product was manufactured between May 2016 and August 2017 with expiration dates between May 2019 and August 2020.
Identify if your Alaris Pump Infusion Set has any of the listed model codes (e.g., 10010453, 10010454, etc.)
Reach out to Becton Dickinson for further assistance if you are unsure about your model code or need help with the recall.
The recall includes model codes such as 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930, and others listed in the record.
Check the model code on your product against the list of affected codes provided in the recall. The product was manufactured between May 2016 and August 2017 with expiration dates between May 2019 and August 2020.
Contact Becton Dickinson directly to confirm if your product is affected and to get instructions on next steps.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1770-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1770-2019 from Becton Dickinson. 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.
