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.
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.
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.
The pumps were not properly inspected before release, which means they might not work as intended. This could cause medication to be delivered too slowly, too quickly, or not at all, potentially causing harm to patients.
Patients using the PERFUSOR SPACE infusion pumps for medication delivery are most at risk. Healthcare providers who use these pumps for syringe infusion therapy may also be affected.
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.
Look for serial numbers 633299, 633307, 633310, 633313, 633315, or 633318 on the pump.
B Braun is recalling US version PERFUSOR SPACE infusion pumps with specific serial numbers due to potential issues with medication delivery accuracy.
Check for serial numbers 633299, 633307, 633310, 633313, 633315, or 633318 on the pump.
The recall record does not specify a remedy, so contact B Braun directly for guidance.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0819-2022 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0819-2022 from B Braun. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
