Medicrea International recalls

Medicrea International has 22 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 21 Jan 2026. 16 are still ongoing. 2 were reported in the last 12 months. The most frequent reason is packaging defects.

Total recalls22since 2020

Last 12 months2reported

Class I00% of total

Ongoing16latest 21 Jan 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 1 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 2Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 22 100%Class III 0 0%

Why medicrea international is recalled

Product types

By year

202629%
202515%
20231150%
2020836%

Ongoing medicrea international recalls

16 active

Reported	Class	Recall	Company	Reason	Where
21 Jan 2026Device	CLASS II	Medicrea, IB3D Universal Implant Inserter recalled	Medicrea International	Other	Nationwide
21 Jan 2026Device	CLASS II	Medicrea, IB3D PL Instruments Set recalled by Medicrea International	Medicrea International	Other	Nationwide
12 Feb 2025Device	CLASS II	UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer recalled	Medicrea International	Device Malfunction	50 states
30 Aug 2023Device	CLASS II	Impix Alif S/a recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	PASS LP recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	Impix Tlif recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide

All medicrea international recalls, newest first

22 total

Reported	Class	Recall	Company	Reason	Where
21 Jan 2026Device	CLASS II	Medicrea, IB3D Universal Implant Inserter recalled	Medicrea International	Other	Nationwide
21 Jan 2026Device	CLASS II	Medicrea, IB3D PL Instruments Set recalled by Medicrea International	Medicrea International	Other	Nationwide
12 Feb 2025Device	CLASS II	UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer recalled	Medicrea International	Device Malfunction	50 states
30 Aug 2023Device	CLASS II	Impix Alif S/a recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	PASS LP recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	Impix Tlif recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	Impix 3D recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	Impix Dlif recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	Impix Manta+ recalled by Medicrea International	Medicrea International	Packaging Defects	Nationwide
30 Aug 2023Device	CLASS II	Granvia-c, REF numbers: a)¿¿¿¿¿ A13111427, b)¿¿¿¿ A13112567 recalled	Medicrea International	Packaging Defects	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.