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Terminated

InterV CurvePlus Kit, REF Numbers: a) INTVMC-15-FLDSK b) INTVMC-20-FLDSK. For use in Orthopedic / spinal procedures.

FDA Recall Z-1753-2021 · Posted None

Recalling FirmZavation
Recall StatusTerminated
Product CodeNDN
Date Initiated2021-03-25
Date Terminated2023-03-20
Product Quantity36 units

Reason for Recall

Products distributed as sterile may not have been adequately sterilized

Firm Action

Zavation initially notified their consignees of the problem by email beginning on 03/24/2021 and requested they quarantine the product. The firm sent a subsequent email beginning on 04/13/2021 requesting the return of the product. The recall is being conducted to the user level.

Root Cause

Vendor change control

Distribution Pattern

US nationwide distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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