Draeger Medical, Inc. 2023-05-24 Health critical FDA
Health · FDA · Recall #FDA-Z-1440-2023
VentStar Basic (P)180, MP00351 Recall
Issued May 24, 2023 · Draeger Medical, Inc.
In May 2023, Draeger Medical, Inc. recalled the VentStar Basic (P)180, MP00351, a critical 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
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
What you should do
- 1 Stop using VentStar Basic (P)180, MP00351 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Draeger 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.
Official remedy (Voluntary):
Recall details
- Brand
- Draeger Medical, Inc.
- Category
- Health
- Recall date
- May 24, 2023
- Units affected
- Not reported
- Sold at
- Domestic: US Nationwide Distribution.
- Recall number
- FDA-Z-1440-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Draeger Medical, Inc. has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.