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Terminated

LivaNova Sorin Connect DPIII KOMPL. S5 REF 96-415-130, 2017-08-15, IPX1, RXOnly, (01)04033817901594 Product Usage: The S5 System is used to perform, control and monitor extracorporeal blood circulation during an operation for up to six hours.

FDA Recall Z-1119-2020 · Posted None

Recalling FirmLivaNova USA Inc.
Recall StatusTerminated
Product CodeDTQ
Date Initiated2019-01-28
Date Terminated2022-01-31
Product Quantity5 Datapads

Reason for Recall

Incorrect labeling; it was identified that some Datapad devices contained incorrect labels. Specifically the manufacturing date in the production identifier was incorrect and the manufacturing date on the unique device identifier label was labeled in the format of yy-mm-dd instead of yyyy-mm-dd.

Firm Action

On 01/28/2019, a Medical Device Correction letter was mailed to affected consignees. The letter asked customers to take the following actions: 1. Please check your inventory using the list of affected products delivered to your facility in Attachment 1; 2. Using the attached Customer Response Form (Attachment 2), please respond by email to [email protected] to confirm that you have affected products in your facility. Your LivaNova reference person will contact you for the replacement of the product labels with labels bearing the correct manufacturing date. 3. Please ensure that this Medical Device Correction is communicated to all personnel within your organization who need to be aware of it. If you have transferred any of the affected devices to a third party, please communicate this information to them and inform the LivaNova Quality Assurance Team at [email protected]. 4. For questions regarding this Medical Device Correction, please contact us at (800) 986-4702 or by e-mail to [email protected].

Root Cause

Error in labeling

Distribution Pattern

US: NJ and CA

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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