Abbott i-STAT EG7+ cartridge-IVD. Intended for the quantitative measurement of sodium, potassium, ionized calcium, pH, pCO2, pO2 and hematocrit in venous, arterial or capillary whole blood. List Number: 03P76-25
FDA Recall Z-0881-2021 · Posted None
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Recalling FirmAbbott Point Of Care Inc.
Recall StatusTerminated
Product CodeCHL
Date Initiated2020-12-22
Date Terminated2023-09-01
Product Quantity1,521,800 cartridges US and 2,641,053 cartridges OUS
Reason for Recall
Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit higher than expected reported results when stored at room temperature (18 to 30C) for periods of time in excess of 3 days for lot numbers *20100 to *20339 and 7 days for lot numbers *20340 and above
Where * = lot letter A, K, L, M, N, W or Y.
Firm Action
Abbott Point of Care notified Customers via email beginning on 22 December 2020. Customer letters will begin shipping via FedEx on 28-December-2020 for delivery on or around 29-December-2020. Letter states reason for recall, health risk and action to take:
While Abbott Point of Care continues to investigate this issue, if reporting ionized calcium is required, it is recommended that the i-STAT CG8+ and EG7+ cartridges be used only:
within 3 days of removal from refrigerated storage for lot numbers between *20100 and *20339
within 7 days of removal from refrigerated storage for lot numbers *20340 and above Where *= lot letter A, K, L, M, N, W and Y
If your facility is unable to manage to the recommended action outlined above, Abbott Point of Care recommends that your facility disable and not report the ionized calcium test on the i-STAT CG8+ and EG7+ cartridges and use an alternate i-STAT cartridge or method for reporting ionized calcium. Please see additional information below on how to disable the ionized calcium test for these cartridges.
Please confirm receipt and understanding of this communication by responding to the business reply form included with this letter.
Additional information regarding potential solutions will be provided separately by APOC. If you have forwardedany i-STAT CG8+ and EG7+ cartridges to another facility, we request that you please provide a copy of this
letter to them.
Your Abbott Point of Care sales and support team will be contacting you to review interim solutions for the challenges this communication may bring. If you have any questions regarding this information, please contact Abbott Point of Care Technical Support at 1-844-256-9531, or via email at [email protected] or visit the Abbott Point of Care website www.pointofcare.abbott. Additionally, please report any questions or concerns about the performance of the ionized calcium test on the i-STAT CG8+ and EG7+ cartridges to Abbott Point of Care Tec
Root Cause
Under Investigation by firm
Distribution Pattern
Nationwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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