Use caution Medical device recall · FDA · Published February 7, 2022

B Braun PERFUSOR SPACE US Version Recall: Infusion Errors Risk

B Braun recalls US version PERFUSOR SPACE infusion pumps with serial numbers 633299-633318 due to potential infusion errors. Affected units may cause delays, overinfusion, or underinfusion of medication.

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

🇺🇸 FDA recall #Z-0819-2022Medical device B Braun ›

Use caution until it’s fixed

Units not properly inspected prior to release to the market, may not function as indicated in the product labeling, resulting in syringe detection and infusion accuracy that can result in delays in therapy, overinfusion, or underinfusion.

Take action

Contact the company

Recalling firmB Braun Medical Inc200 Boulder Dr · Breinigsville, PA 18031-1532

✎ GovInfoNow plain-language explainer

B Braun is recalling US version PERFUSOR SPACE infusion pumps with specific serial numbers because they may not function correctly, leading to medication delays, overinfusion, or underinfusion risks. This could affect patients receiving infusion therapy. Read more at govinfonow.com/recall/61176-b-braun-perfusor-space-us-version-recall-infusion-errors-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/61176-b-braun-perfusor-space-us-version-recall-infusion-errors-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0819-2022

Cite this page

“B Braun PERFUSOR SPACE US Version Recall: Infusion Errors Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61176-b-braun-perfusor-space-us-version-recall-infusion-errors-risk. Based on FDA recall #Z-0819-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0819-2022%22&limit=1).

B Braun Medical Inc recalled the PERFUSOR SPACE - US VERSION syringe infusion pump on Feb. 7, 2022, according to the FDA. The hazard involves units not properly inspected prior to release, which may result in delays in therapy, overinfusion, or underinfusion.

How to tell if you have it

Brand: B Braun
Product: PERFUSOR SPACE - US VERSION
Catalog Number: 8713030U
Serial Numbers: 633299, 633307, 633310, 633313, 633315, 633318
GUIDID: 04046963716745

The hazard

Units not properly inspected prior to release to the market may not function as indicated in the product labeling. This can result in syringe detection and infusion accuracy issues that lead to delays in therapy, overinfusion, or underinfusion.

Context

GovInfoNow's records show B Braun Medical Inc has 66 other recalls on record since Oct. 15, 2013. Other recent recalls of similar products include a Baxter Novum IQ Syringe Pump recall for software issues (Aug. 11, 2026) and an ICU Medical Plum Duo Infusion Pump recall for under/over-delivery risk (April 29, 2026).

How to tell if you have this one

Check for serial numbers 633299, 633307, 633310, 633313, 633315, or 633318 on the pump. The US version of PERFUSOR SPACE is intended for syringe infusion pumps that configure customized medication solutions.

Brand
B Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Numbers
Look for serial numbers 633299, 633307, 633310, 633313, 633315, or 633318 on the pump.

Where it went and when

Where it was distributed

Distributed in Massachusetts and Vermont.

FDA distribution: “US Distribution to states of: MA, VT” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Massachusetts, Vermont.

Recall timeline

FDA terminated this recall 23 months after the firm started it.

Feb 7, 2022Firm started the recall
Mar 22, 2022FDA classified it Class II
Mar 30, 2022Published in FDA’s Enforcement Report
Dec 28, 2023FDA terminated the recall

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

Similar recalls

Latest medical device recalls

Keep exploring

More B Braun recalls

Link to this recall

<a href="https://govinfonow.com/recall/61176-b-braun-perfusor-space-us-version-recall-infusion-errors-risk">B Braun PERFUSOR SPACE US Version Recall: Infusion Errors Risk (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-0819-2022 (February 7, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0819-2022 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.