Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2459-2023 — GRANVIA-C, REF numbers: a)¿¿¿¿¿ A13111427, b)¿¿¿¿ A13112567, c)¿¿¿¿¿ A13113456, d)¿¿¿¿ A13131516, e)¿¿¿¿ A13131789, f)¿¿¿¿¿¿ A13132012, g)¿¿¿¿¿ B13111014, h)¿¿¿¿ B13111015, i)¿¿¿¿¿¿ B13111016, j)¿¿¿¿¿¿ B13111017, k)¿¿¿¿¿ B13111025, l)¿¿¿¿¿¿ B13111026, m)¿¿¿ B13111027, n)

U.S. FDA — Device Enforcement · France · 2023-07-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2459-2023
Date of alert
2023-07-12
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
Medicrea International
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
03613720235637
Reported risk: There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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