Reported Aug 30, 2023 · Ongoing

GRANVIA-C, REF numbers: a)¿¿¿¿¿ A13111427, b)¿¿¿¿ A13112567, c)¿¿¿¿¿ A13113456, d)¿¿¿¿ A13131516, e)¿¿¿¿ A13131789,…

Medicrea International

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medicrea International · Vancia · Rillieux La Pape, N/A · N/A

Is this the product you have?

  • 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)¿¿¿¿ B13111034
    • o)¿¿¿¿ B13111035
    • p)¿¿¿¿ B13111036
    • intervertebral fusion device - cervical
Lot codes and dates

16 of 16 products

Products covered by this recall
Model / numberBarcodesProduct as published
03613720235637¿¿¿¿¿ A13111427, , Lot Numbers: 19D0379, 19J0745, 20F0921
03613720235651¿¿¿¿ A13112567, , Lot Numbers: 18F0191, 19D0380
03613720235668.03613720235668¿¿¿¿¿ A13113456, Lot Numbers: 19C0241, 20F0929
03613720235682¿¿¿¿ A13131516, , Lot Numbers: 21A0438
03613720235699¿¿¿¿ A13131789, , Lot Numbers: 21D0856
03613720235705¿¿¿¿¿¿ A13132012, , Lot Numbers: 21D0857
03613720192602¿¿¿¿¿ B13111014, , Lot Numbers: 18J0704, 19I0437, 19L0317, 20B0743, 20H0170, 20I0346
03613720192619¿¿¿¿ B13111015, , Lot Numbers: 18A0891, 18L0331, 19B0305, 19D0744, 19G0689, 19I0840, 19K0222, 20A0967, 20B0167, 20I0201, 20J0513, 21A0098
03613720192626¿¿¿¿¿¿ B13111016, , Lot Numbers: 18J0705, 19C0759, 19I0435, 19L0103, 20G0353, 20K0398, 21A0099, 21A0574, 21F0151
03613720192633¿¿¿¿¿¿ B13111017, , Lot Numbers: 18J0706, 21D0097, 21I0125
03613720192664¿¿¿¿¿ B13111025, , Lot Numbers: 18D0593, 19A0658, 19C0394, 19K0343, 20J0514
03613720192671¿¿¿¿¿¿ B13111026, , Lot Numbers: 18J0707, 20J0516, 21I0072
03613720192688¿¿¿ B13111027, , Lot Numbers: 18J0709, 21A0575, 21I0126
03613720192718¿¿¿¿ B13111034, , Lot Numbers: 18B1066, 18D0594, 18E0614, 18H0671, 18K0878, 18L0389, 19A0354, 19A0377, 19D0306, 19D0307, 19D0578, 19E0387, 19J0465, 19K0068, 19L0607, 20B0744, 20G0354, 20K0399, 21A0203, 21A0732, 21F0153
03613720192725¿¿¿¿ B13111035, , Lot Numbers: 18A0892, 18J0465, 18J0710, 19A0355, 19B0304, 19B0394, 19B0395, 19D0579, 19F0100R, 19J0466, 19K0069, 19L0394, 20B0745, 20C0296, 20G0355, 20I0348, 20K0434, 21A0103
03613720192732¿¿¿¿ B13111036, , Lot Numbers: 18B1067, 18F1031, 18J0466, 18J0711, 18L0390, 19A0356, 19B0915, 19D0581, 19G0690, 19K0157, 19L0804, 20E0256, 20I0349, 20J0512, 21A0104
Amount recalled
O (US)

This recall covers 11 products

The agency filed one notice per product. You are reading one of them; the other 10 are below.

Where it was sold

  • Nationwide

Why it was recalled

There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.