Oxy2Mask
Brand(s)
Last updated
Summary
Product
Oxy2Mask
Issue
Medical devices - Device compatibility
What to do
Contact the manufacturer if you require additional information.
Affected products
Affected products | Lot or serial number | Model or catalog number/ |
---|---|---|
Oxy2Mask O2/ETCO2 | W98170 W1001335 W1001104 | OP-2125-8 OP-2125-14 OP-2125-8SLM |
Oxy2Pro | W1003251 | PRM-2110-8F |
Oxy2Mask O2/ETCO2 | W96157 W1001100 W1001102 W1001332 W1003502 | OM-2125-14 OM-2125-8SLM OM-2125-8 OM-2125-14SLM |
Oxy2Mask O2/ETCO2 | W96158/VAL W1001330 | OK-2125-8SLM OK-2125-8 |
Oxy2Pro | W1001948 W1003244 W99427 | PRM-2110-8M |
Oxy2Pro | W99426 | PRP-2110-8F |
Oxy2Pro | W1001949 | PRP-2110-8M |
Issue
There is a potential for the elbow component to not be securely connected to the diffuser component. This originated from a complaint received on November 15, 2023.
Recall start date: January 5, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies
Southmedic Inc.
50 Alliance Blvd, Barrie, Ontario, Canada, L4M 5K3
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-74934
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