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Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700(IPN917285), cardiac pump - safety alert
Official notice
21 Dec 2022
Last checked
21 Dec 2022
An official FDA notice concerns Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700(IPN917285), cardiac pump - safety alert. An official FDA notice concerns Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700(IPN917285), cardiac pump. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2022-12-21. Lots: /Serial. Recall numbers: Z-0439-2023. Check the official notice for the complete list. Published 2022-12-21.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Recall number
Z-0439-2023
Official notice
2022-12-21
The hazard
The hazard
An official FDA notice concerns Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700(IPN917285), cardiac pump. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2022-12-21. Lots: /Serial. Recall numbers: Z-0439-2023. Check the official notice for the complete list.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Lots
Event Ids
Recall Numbers
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Affected area 2
Company & contacts
Company & contacts
Brand: Arrow. Contact: ARROW INTERNATIONAL Inc..
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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