Draeger Medical, Inc. recalls Carina Sub-Acute Care Ventilator
See all recalls from Draeger Medical, Inc. →Recalled Product
Carina Sub-Acute Care Ventilator
Hazard / Issue
Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Part No. 5704110; UDI-DI 04048675398516; All Serial No.
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Carina Sub-Acute Care Ventilator →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime