Global Anesthesia Devices Market: Restraints
Increasing product recall due to serious injuries or death is one of the major factor restraining the growth of global anesthesia market over the forecast. For instance, in September 2021, Armstrong Medical Limited, a manufacturer of hospital equipment, recalls AMSORB PLUS PREFILLED G-CAN 1.0L(AMSORB PLUS is a chemical substance used in anesthesia machines to absorb carbon dioxide (CO2) the patient breathes out while under anesthesia. This substance is provided in a prefilled canister (Prefilled G-CAN 1.0L) that is attached to the ventilator/anesthesia machine.) due to reduced gas flow to patients during anesthesia. The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. The difficulties in flow may cause a failure in the pre-use or “CHECK-OUT” test on the anesthesia machine. It may also occur when a patient is already under anesthesia if an affected canister is attached to the anesthesia machine while a patient is already under anesthesia.
Anesthesia Device Market Report Snapshots
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