Spineart recalls

Spineart has 13 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 20 Aug 2025. 4 are still ongoing. The most frequent reason is potency & assay.

Total recalls13since 2018

Last 12 months0reported

Class I00% of total

Ongoing4latest 20 Aug 2025

Recalls per month, last 24 months

click a bar for that month

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

Severity split

Class I 0 0%Class II 12 92%Class III 1 8%

Why spineart is recalled

Product types

By year

2025215%
202418%
202318%
202118%
201918%
2018754%

Ongoing spineart recalls

4 active

Reported	Class	Recall	Company	Reason	Where
20 Aug 2025Device	CLASS II	Perla ¿ Tl Mis Cannulated Fenestrated Polyaxial Screw recalled	Spineart	Labeling Errors	Nationwide
20 Aug 2025Device	CLASS II	Perla ¿ Tl Mis Cannulated Fenestrated Polyaxial Screw recalled	Spineart	Labeling Errors	Nationwide
15 May 2024Device	CLASS II	Perla Tl 25d Screw recalled by Spineart	Spineart	Other	Nationwide
3 May 2023Device	CLASS II	Juliet Ti LL, Lateral Lumbar Ti-life Plate Small recalled by Spineart	Spineart	Other	Nationwide

All spineart recalls, newest first

13 total

Reported	Class	Recall	Company	Reason	Where
20 Aug 2025Device	CLASS II	Perla ¿ Tl Mis Cannulated Fenestrated Polyaxial Screw recalled	Spineart	Labeling Errors	Nationwide
20 Aug 2025Device	CLASS II	Perla ¿ Tl Mis Cannulated Fenestrated Polyaxial Screw recalled	Spineart	Labeling Errors	Nationwide
15 May 2024Device	CLASS II	Perla Tl 25d Screw recalled by Spineart	Spineart	Other	Nationwide
3 May 2023Device	CLASS II	Juliet Ti LL, Lateral Lumbar Ti-life Plate Small recalled by Spineart	Spineart	Other	Nationwide
7 Jul 2021Device	CLASS II	Perla TL Lateral Connector Open recalled by Spineart	Spineart	Labeling Errors	Nationwide
4 Dec 2019Device	CLASS III	Intersomatic Juliet Ti OL cage recalled by Spineart	Spineart	Device Malfunction	CA
24 Jan 2018Device	CLASS II	Tryptik(r) 2 C-plate Self-tapping Polyaxial Screw, Length recalled	Spineart	Potency & Assay	CA
24 Jan 2018Device	CLASS II	Tryptik(r) 2 C-plate Self-tapping Polyaxial Screw, Length recalled	Spineart	Potency & Assay	CA
24 Jan 2018Device	CLASS II	Tryptik(r) 2 C-plate Self-tapping Polyaxial Screw, Length recalled	Spineart	Potency & Assay	CA
24 Jan 2018Device	CLASS II	Tryptik(r) 2 C-plate Self-tapping Polyaxial Screw, Length recalled	Spineart	Potency & Assay	CA

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.