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Pump Modules Recall Due to May have been serviced with previously recalled be...

# Major Recall Alert: Pump Modules Recalled Due to Previously Recalled Bezel Kit Assemblies

Patients and healthcare providers, take note: BD (Becton, Dickinson and Company) has issued an urgent **voluntary recall** for **Alaris™ and BD Alaris™ Pump Modules**. These medical devices may have been serviced with previously recalled bezel kit assemblies, posing significant safety risks. Here’s what you need to know about this recall and the actions you should take immediately to stay safe.

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## Why This Recall Is Important

Medical device recalls are rare, but when they happen, swift awareness is critical. In this case, BD has identified that **bezel kit assemblies manufactured between April 2011 and June 2017**, previously recalled in 2019, are still in use by some third-party service providers.

These bezel kits were manufactured with **plastic material (FR-110 bezels)** that weakens over time, potentially causing:

- **Separation or breakage of bezel bosses**, resulting in:
- Free flow of medication
- Over-infusion or under-infusion
- Interruption of infusion

These malfunctions could lead to **serious patient injuries or even death**, making it essential for anyone using these devices to act immediately.

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## Details of the Recall

BD issued this voluntary recall notice on **July 15, 2025**, targeting **Alaris™ and BD Alaris™ Pump Modules** (model 8100) that may have been serviced with defective spare parts. While the original devices may not have been manufactured with faulty bezels, **third-party or customer servicing** is believed to have introduced these recalled components.

### Key Information:
- **Affected Components**: FR-110 bezel kit assemblies manufactured between April 2011 and June 2017
- **Original Recall**: Introduced in 2019
- **Current Concern**: Affected bezels remain in circulation through customer/third-party servicing
- **Reported Consequences**: Incidents of serious injury and patient fatalities

### BD advises:
- **Dispose of any affected bezel kit assemblies** immediately if in possession.
- **Inspect pump modules** to check for affected bezels—remove from service immediately if found.
- **Contact BD for next steps**: BD Customer Support is available at **1-888-562-6018**.

For more information, visit the official FDA recall page here: [FDA Recall Notice](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-update-voluntary-global-recall-alaristm-and-bd-alaristm-pump-modules-serviced-legacy-bezel).

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## What You Should Do

If you currently use or service **Alaris™ and BD Alaris™ Pump Modules**, take the following actions to ensure safety:

1. **Perform a thorough visual inspection** of all pump modules.
2. Identify if your devices were serviced using affected bezel kit assemblies.
3. **Immediately remove affected pumps from use**.
4. **Dispose of recalled parts** to prevent future servicing incidents.
5. Report any issues or concerns to BD’s Complaint Center by:
- Calling **1-844-823-5433** (Mon–Fri, 9 a.m.–6 p.m. ET)
- Emailing **productcomplaints@bd.com**

Additionally, patients and healthcare workers can report adverse reactions or events associated with these devices to the **FDA MedWatch Program**.

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## Stay Safe – Get Instant Recall Alerts

**Don’t take chances with your health or medical devices.** With recalls like this one, early action can prevent serious harm. Stay informed by subscribing to recall alerts and notifications. Protect yourself and your loved ones from potential risks by accessing real-time safety notifications directly from trusted sources.

### **Download Our App for Instant Recall Alerts!**
Stay one step ahead with up-to-date recall notifications for medical devices, food, and other consumer products. Be proactive—download our free app today and get peace of mind knowing you’re always informed.

For additional resources and updates about this recall, visit the official BD website or follow BD on social media:
- LinkedIn: [BD LinkedIn](https://www.linkedin.com/company/bd1/)
- Twitter: [@BDandCo](https://www.twitter.com/BDandCo)
- Instagram: [@becton_dickinson](https://www.instagram.com/becton_dickinson)

**Source**: [FDA Official Recall Notification](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-update-voluntary-global-recall-alaristm-and-bd-alaristm-pump-modules-serviced-legacy-bezel)

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