Reported Jul 31, 2024 · Ongoing
Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump System Model/Catalog Number: 8713030U Product…
B Braun Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B Braun Medical Inc · 200 Boulder Dr · Breinigsville, PA · 18031-1532
Is this the product you have?
- Brand NamePerfusor
- Space Product NamePerfusor Space Infusion
- Pump System Model/Catalog Number8713030U
- Product DescriptionPerfusor Space Infusion Pump System, Infusion Pump, 1
- each ComponentN/A
- Lot codes and dates
- Lot Code
Model No 8713030UUDI-DI 4046963716745All Serial Numbers
- Lot Code
- Amount recalled
- 14949
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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