Peter Lazic recalls

Peter Lazic has 5 recalls on record with the FDA and USDA, the earliest in 2024 and the latest reported on 20 Mar 2024. 5 are still ongoing.

Total recalls5since 2024

Last 12 months0reported

Class I00% of total

Ongoing5latest 20 Mar 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 5 100%Class III 0 0%

Why peter lazic is recalled

Other Reasons360%
Sterility240%

Product types

Other Medical Devices5100%

By year

20245100%

Ongoing peter lazic recalls

5 active

Reported	Class	Recall	Company	Reason	Where
20 Mar 2024Device	CLASS II	D-Clip Standard/Mini Applier bayonet, jaw rigid, double action recalled	Peter Lazic	Other	Nationwide
20 Mar 2024Device	CLASS II	L-Aneurysm Clip Titanium Paddle-Clip, permanent straight recalled	Peter Lazic	Sterility	Nationwide
20 Mar 2024Device	CLASS II	D-Clip Standard/Mini Applier bayonet, jaw rigid, double action recalled	Peter Lazic	Other	Nationwide
20 Mar 2024Device	CLASS II	D-Clip Standard/Mini Applier bayonet, jaw rigid, double action recalled	Peter Lazic	Other	Nationwide
20 Mar 2024Device	CLASS II	L-Aneurysm Clip Titanium Paddle-Clip, permanent straight, Sterile recalled	Peter Lazic	Sterility	Nationwide

All peter lazic recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
20 Mar 2024Device	CLASS II	D-Clip Standard/Mini Applier bayonet, jaw rigid, double action recalled	Peter Lazic	Other	Nationwide
20 Mar 2024Device	CLASS II	L-Aneurysm Clip Titanium Paddle-Clip, permanent straight recalled	Peter Lazic	Sterility	Nationwide
20 Mar 2024Device	CLASS II	D-Clip Standard/Mini Applier bayonet, jaw rigid, double action recalled	Peter Lazic	Other	Nationwide
20 Mar 2024Device	CLASS II	D-Clip Standard/Mini Applier bayonet, jaw rigid, double action recalled	Peter Lazic	Other	Nationwide
20 Mar 2024Device	CLASS II	L-Aneurysm Clip Titanium Paddle-Clip, permanent straight, Sterile recalled	Peter Lazic	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.