Date Initiated by Firm | March 25, 2022 |
Create Date | May 19, 2022 |
Recall Status1 |
Terminated 3 on October 05, 2023 |
Recall Number | Z-1117-2022 |
Recall Event ID |
90011 |
Product Classification |
Generator, oxygen, portable - Product Code CAW
|
Product | CAIRE FreeStyle Comfort Portable Oxygen Concentrator with autoSAT, UltraSense and autoDOSE, model #AS200-3 |
Code Information |
Serial numbers CBB5221200337 and CBB5221200287. |
Recalling Firm/ Manufacturer |
Caire, Inc. 2200 Airport Industrial Dr Ste 500 Ball Ground GA 30107-4686
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For Additional Information Contact | Sheril Ray 770-721-7719 |
Manufacturer Reason for Recall | The device was not cleared for U.S. distribution. |
FDA Determined Cause 2 | No Marketing Application |
Action | The recalling firm initially contacted the customer via voicemail and email on 3/25/2022. The email informed the consignee that the two affected units that were shipped to them could not be sold in the U.S. or its territories due to FDA approval. The email requested the consignee confirm their address so that call tags could be sent to them for return of the affected units. The consignee was informed the units will be replaced with the new AS200-1 units as soon as the recalled units are returned. The model and serial numbers were provided of the affected units. The voicemail message summarized the information that was in the email. |
Quantity in Commerce | 2 oxygen concentrators |
Distribution | Distribution was made to Puerto Rico. There was no foreign/government/military distribution. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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