Fabius Tiro recall
Fabius Tiro, anesthesia machine, catalog no. 8606000 Product Usage: The products are inhalation anesthesia machines for use in operating, induction…
Why was Fabius Tiro recalled?
The automatic ventilation may fail if the position detection of the motor is disturbed. If the ventilator cover is damaged, manual ventilation may also fail.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial no: ASKJ-0195 ASKK-0079 ASKF-0226 ASKF-0227 ASKF-0228 ASKF-0229 ASKF-0230 ASKH-0086 ASKH-0071 ASKJ-0177 ASKK-0020 ASKK-0021 ASKH-0053 ASKH-0054 ASKH-0055 ASKH-0056 ASKH-0057 ASKH-0067 ASKH-0068 ASKH-0063 ASKH-0065 ASKH-0064 ASKH-0130 ASKH-0131 ASKJ-0173 ASKH-0031
- Product
- Fabius Tiro, anesthesia machine, catalog no. 8606000 Product Usage: The products are inhalation anesthesia machines for use in operating, induction…
- Recalling firm
- Draeger Medical, Inc.
- Quantity
- 26
- Distribution
- US Nationwide Distribution to accounts in 21 states: AZ, CA, CO, ID, IL, KS, MA, MI, MS, NC, NY, OH, OK, PA, RI, TN, TX, UT, VA, WA, WI; and PR.
- Recall date
- May 16, 2018
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)