Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless … Recall
Issued July 31, 2024 · B Braun Medical Inc
In July 2024, B Braun Medical Inc recalled the Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless …, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact B Braun Medical Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- B Braun Medical Inc
- Category
- Health
- Recall date
- July 31, 2024
- Units affected
- Not reported
- Sold at
- Domestic distribution nationwide. International distribution to Canada.
- Recall number
- FDA-Z-2434-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- B Braun Medical Inc has 23 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.