Zimmer Biomet Spine recalls

Zimmer Biomet Spine has 8 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 10 Jan 2024. 1 is still ongoing. The most frequent reason is sterility.

Total recalls8since 2016

Last 12 months0reported

Class I00% of total

Ongoing1latest 10 Jan 2024

Recalls per month, last 24 months

click a bar for that month

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

Severity split

Class I 0 0%Class II 8 100%Class III 0 0%

Why zimmer biomet spine is recalled

Product types

By year

2024113%
2019338%
2017225%
2016225%

Ongoing zimmer biomet spine recalls

1 active

Reported	Class	Recall	Company	Reason	Where
10 Jan 2024Device	CLASS II	Vitality Polyaxial Screw, 5mmx recalled by Zimmer Biomet Spine	Zimmer Biomet Spine	Lead & Heavy Metals	Nationwide

All zimmer biomet spine recalls, newest first

8 total

Reported	Class	Recall	Company	Reason	Where
10 Jan 2024Device	CLASS II	Vitality Polyaxial Screw, 5mmx recalled by Zimmer Biomet Spine	Zimmer Biomet Spine	Lead & Heavy Metals	Nationwide
6 Mar 2019Device	CLASS II	Vitality¿ Spinal Fixation System recalled by Zimmer Biomet Spine	Zimmer Biomet Spine	Sterility	Nationwide
6 Mar 2019Device	CLASS II	Vitality¿ Spinal Fixation System recalled by Zimmer Biomet Spine	Zimmer Biomet Spine	Sterility	Nationwide
6 Mar 2019Device	CLASS II	Vitality¿ Spinal Fixation System.Spinal Intervertebral recalled	Zimmer Biomet Spine	Sterility	Nationwide
14 Jun 2017Device	CLASS II	Vitality Spinal Fixation System recalled by Zimmer Biomet Spine	Zimmer Biomet Spine	Potency & Assay	Nationwide
5 Apr 2017Device	CLASS II	Altius M-ini OCT Posterior Spinal Fixation System recalled	Zimmer Biomet Spine	Potency & Assay	Nationwide
17 Aug 2016Device	CLASS II	Zyston¿ Transform Implant Kit recalled by Zimmer Biomet Spine	Zimmer Biomet Spine	Sterility	Nationwide
17 Aug 2016Device	CLASS II	Zyston¿ Transform Instrument Case recalled by Zimmer Biomet Spine	Zimmer Biomet Spine	Sterility	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.