FDA Device Intelligence
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Absorbent, Carbon-Dioxide

FDA product code CBL · Class 1 · Anesthesiology

134
Registered devices
206
Adverse events
7
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-08-05Armstrong Medical Services LimitedSome devices may be associated with high and unexpected resistance to gas flow during clinical use, impacting or preventing adequate ventilation of an anaesthet
2010-10-20Darex Container Products Div of W.R. Grace & Co.Pre-Pak units of SODASORB CO2 absorbent manufactured prior to August 2010 may have missing or illegible expiration dates and/or batch numbers.
2010-10-20Darex Container Products Div of W.R. Grace & Co.Pre-Pak units of SODASORB CO2 absorbent manufactured prior to August 2010 may have missing or illegible expiration dates and/or batch numbers.
2010-08-12Allied Healthcare Products IncThe granules do not absorb as long as expected in the anesthesia machines
2005-03-31Darex Container Products Div of W.R. Grace & Co.Both lots were found to be out of specification due to an elevated level of small particles (fines).
2003-02-11Darex Container Products Div of W.R. Grace & Co.Contaminated with epoxy chips.
2003-02-11Darex Container Products Div of W.R. Grace & Co.Contaminated with epoxy chips.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.