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Use caution Medical device recall · FDA · Published June 14, 2024

B Braun Perfusor Space Syringe Pump Recall: Incompatible Monoject Syringes Risk Overdose

B Braun recalls Perfusor Space wireless syringe pumps with model 8713031U software due to incompatibility with Cardinal Health Monoject syringes, risking overdose or underdose in medical use.

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

🇺🇸 FDA recall #Z-2434-2024Medical deviceB Braun ›
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Contact the company

Recalling firmB Braun Medical Inc200 Boulder Dr · Breinigsville, PA 18031-1532
✎ GovInfoNow plain-language explainer

B Braun is recalling Perfusor Space wireless syringe pumps with model number 8713031U software because they may not work properly with Cardinal Health Monoject syringes. This could lead to incorrect medication dosing, potentially causing overdose or underdose in medical treatments. Read more at govinfonow.com/recall/54836-b-braun-perfusor-space-syringe-pump-recall-incompatible-monoject-syringes.

Source Summary by GovInfoNow · govinfonow.com/recall/54836-b-braun-perfusor-space-syringe-pump-recall-incompatible-monoject-syringes · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2434-2024

Cite this page

“B Braun Perfusor Space Syringe Pump Recall: Incompatible Monoject Syringes Risk Overdose.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54836-b-braun-perfusor-space-syringe-pump-recall-incompatible-monoject-syringes. Based on FDA recall #Z-2434-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2434-2024%22&limit=1).

B Braun Medical Inc. recalled the Perfusor Space Syringe Pump, Wireless (Model 8713031U) due to compatibility issues with Cardinal Health Monoject syringes that may cause overdose or underdose, according to the FDA on June 14, 2024.

How to tell if you have it

  • Brand: B Braun
  • Product Name: Perfusor Space Syringe Pump, Wireless
  • Model/Catalog Number: 8713031U
  • Software Version: 8713031U
  • Lot Code: Model No 8713031U
  • UDI-DI: 4046964797958
  • All Serial Numbers

The hazard

Changes to manufacturing for Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance. These issues can lead to overdose, underdose, delay in therapy, or delays in occlusion alarms and feeding.

Context

GovInfoNow's records show B Braun Medical Inc has 66 other recalls on record since October 15, 2013. Recent similar recalls include a Baxter Novum IQ Syringe Pump recall for software issues causing infusion errors on August 11, 2026, and a Cardinal Health Monoject Tuberculin Syringe recall for wrong insulin syringes in packaging on February 27, 2026.

How to tell if you have this one

Check for the model number 8713031U on the pump's label. The software version should also be 8713031U. These pumps were sold with Cardinal Health Monoject syringes for infusion therapy.

  • Brand
    B Braun
  • Category
    Medical device
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Domestic distribution nationwide. International distribution to Canada.
Recall numberProduct, codes & lotsQuantity
Z-2433-2024Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump System Model/Catalog Number: 8713030U Product Description: Perfusor Space Infusion Pump System, Infusion Pump, 1 each Component: N/A; Lot Code: Model No 8713030U; UDI-DI 4046963716745; All Serial Numbers14949
Z-2434-2024Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless Model/Catalog Number: 8713031U Software Version: 8713031U Product Description: Perfusor Space Syringe Pump, Infusion Pump, 1 each Component: N/A; Lot Code: Model No 8713031U; UDI-DI 4046964797958; All Serial Numbers9943
Z-2435-2024Brand Name: Perfusor Space Product Name: Perfusor PCA Syringe Pump Model/Catalog Number: 8713080U Product Description: Perfusor¿ Space Syringe Pump, Infusion Pump, 1 each Component: N/A; Lot Code: Model No 8713080U; UDI-DI 4046963915308; All Serial Numbers1663
Z-2436-2024Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT Model/Catalog Number: 8713040U Product Description: Perfusor Space, Infusion Pump Kit, 1 each Component: N/A; Lot Code: Model No 8713040U; UDI-DI 4046963687182; All Serial Numbers930
Z-2437-2024Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Non-Wireless Model/Catalog Number: 8713032U Product Description: Perfusor Space Syringe Pump, Non-Wireless, Infusion Pump, 1 each Component: N/A; Lot Code: Model No 8713032U; UDI-DI 04046964797965; All Serial Numbers4519
Based on the official FDA remedy

What to do — step by step

  1. Check Syringe Compatibility

    Ensure the syringe is compatible with the Perfusor Space pump by verifying it is not a Cardinal Health Monoject syringe.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Domestic distribution nationwide. International distribution to Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 47 days after the firm started it.

1. Firm started the recall: Jun 14, 202412. FDA classified it Class II: Jul 25, 202423. Published in FDA’s Enforcement Report: Jul 31, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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

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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-2434-2024 (June 14, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2434-2024 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA