IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar

Is this the product you have?

• IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar

Lot codes and dates

• GTIN 03613720264439
• Lot Numbers
  • 18I0824
  • 19L0046

Amount recalled

5 units

This recall covers 11 products

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

• IMPIX 3D, REF numbers: a) B242C09122810, b) B242C10062810, c) B242C10122810, d)…
• IMPIX ALIF, REF numbers: a) B15111209, b) B15111212, c) B15111409, d) B15111412
• IMPIX DLIF, REF numbers: a) B16123509, b) B16123511, c) B16124009, d) B16124013, e)…
• IMPIX MANTA, REF numbers: a) A20150407, b) A20250407, c) A20350567, d) B20181743, e)…
• IMPIX TLIF, REF numbers: a) B15130607S, b) B15130609S, c) B15130611S, d) B15130613S, e)…
• PASS LP, REF numbers: a) B02315535Z, b) B02315540Z, c) B02315545Z, d) B02315550Z, e)…
• GRANVIA-C, REF numbers: a)¿¿¿¿¿ A13111427, b)¿¿¿¿ A13112567, c)¿¿¿¿¿ A13113456, d)¿¿¿¿…
• IMPIX C+, REF numbers: a) B20240104, b) B20240105, c) B20240106, d) B20240107, e)…
• IMPIX S, REF numbers: a) B15328071S, b) B15328073S, c) B15328074S, d) B15334072S, e)…
• IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e)…

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.