Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump Recalled by B Braun Medical Inc Due to Units not properly inspected prior to release to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B Braun Medical Inc directly.
Affected Products
PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions Catalog Number: 8713030U
Quantity: 6 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 2 states: MA, VT
About B Braun Medical Inc
B Braun Medical Inc has 148 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report