Use caution Medical device recall · FDA · Published March 26, 2021

Infusion Pump Repair Model 8100: Cracking Bezel Repair Parts Risk Over Infusion

Infusion Pump Repair Model 8100 pumps serviced with non-original bezel repair parts between Jan 2021 and March 2021 may crack, causing infusion interruptions. Affected units have specific serial numbers.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1544-2021Medical device Infusion Pump Repair ›

Use caution until it’s fixed

Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.

Take action

Contact the company

Recalling firmInfusion Pump Repair18 Technology Dr Ste 133 · Irvine, CA 92618-2311

✎ GovInfoNow plain-language explainer

Infusion Pump Repair's Model 8100 infusion pumps that were serviced with non-original bezel repair parts between January 2021 and March 2021 are recalled. Cracking of these repair parts could cause infusion interruptions, potentially leading to over or under infusion of medication. Read more at govinfonow.com/recall/62899-infusion-pump-repair-model-8100-cracking-bezel-repair-parts-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/62899-infusion-pump-repair-model-8100-cracking-bezel-repair-parts-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1544-2021

Cite this page

“Infusion Pump Repair Model 8100: Cracking Bezel Repair Parts Risk Over Infusion.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62899-infusion-pump-repair-model-8100-cracking-bezel-repair-parts-risk. Based on FDA recall #Z-1544-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1544-2021%22&limit=1).

The FDA announced on March 26, 2021, that Infusion Pump Repair is recalling Alaris Pump Module Model 8100 units serviced with an impacted bezel repair part. The agency stated the recall was voluntary and initiated by the firm.

How to tell if you have it

Brand: Infusion Pump Repair
Product: Alaris Pump Module, Model 8100
Distribution: California
Sale Order/Serial Numbers: 1599930872/12335834, 13617863, 13447266, 13089105, 12333728, 13616451, 13618575, 12729374; 82943/4122252, 4122320; 01112101A/12638236, 13813590, 12639090, 13744738, 9951014
Units affected: 15

The hazard

According to the FDA, bezel repair parts used to service and repair infusion pump modules may experience cracking or separation of the posts from the bezel over time. This separation may result in free flow, over infusion, under infusion, or interruption of infusion.

Context

GovInfoNow's records show Infusion Pump Repair has been involved in other recent recalls of similar products, including the Fresenius Kabi LVP-0004 Infusion Pump Recall (2026-02-04) and the B. Braun Medical Spinal Epidural Pump Model 530184 Recall (2026-01-29). Other recent recalls of similar products include the Baxter Novum IQ Syringe Pump Recall (2026-08-11).

How to tell if you have this one

Check if your pump was serviced by Infusion Pump Repair between January 15, 2021 and March 14, 2021. Look for specific serial numbers listed in the recall notice.

Brand
Infusion Pump Repair
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Pump Serial Number
Compare your pump's serial number with the list of affected units provided in the recall notice.
Contact Manufacturer
Reach out to Infusion Pump Repair to confirm if your pump is affected and get instructions for next steps.

Where it went and when

Where it was distributed

Distributed in California.

FDA distribution: “California” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA published this recall 54 days after the firm started it.

Mar 26, 2021Firm started the recall
May 10, 2021FDA classified it Class I
May 19, 2021Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/62899-infusion-pump-repair-model-8100-cracking-bezel-repair-parts-risk">Infusion Pump Repair Model 8100: Cracking Bezel Repair Parts Risk Over Infusion (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-1544-2021 (March 26, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1544-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.