Leica Biosystems Richmond recalls

Leica Biosystems Richmond has 9 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 20 Sep 2017. The most frequent reason is temperature abuse.

Total recalls9since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 20 Sep 2017

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 7 78%Class III 2 22%

Why leica biosystems richmond is recalled

Product types

Test Kits & Diagnostics889%
Other Medical Devices111%

By year

2017778%
2016222%

All leica biosystems richmond recalls, newest first

9 total

Reported	Class	Recall	Company	Reason	Where
20 Sep 2017Device	CLASS II	Cell Marque, Microphthalmia Transcription Factor (MiTF) (C5/D5 Mab.) recalled	Leica Biosystems Richmond	Temperature Abuse	Nationwide
20 Sep 2017Device	CLASS II	Cell Marque, MSH6 (44 Mab.) recalled by Leica Biosystems Richmond	Leica Biosystems Richmond	Potency & Assay	Nationwide
20 Sep 2017Device	CLASS II	Cell Marque, SOX-10 (Polyclonal) recalled by Leica Biosystems Richmond	Leica Biosystems Richmond	Temperature Abuse	Nationwide
20 Sep 2017Device	CLASS II	Cell Marque, Napsin A (MRQ-60 Mab.) recalled	Leica Biosystems Richmond	Temperature Abuse	Nationwide
20 Sep 2017Device	CLASS II	Cell Marque, Podoplanin (D2-40 Mab) recalled	Leica Biosystems Richmond	Temperature Abuse	Nationwide
20 Sep 2017Device	CLASS II	Cell Marque, Glypican-3 (1G12 Mab) recalled by Leica Biosystems Richmond	Leica Biosystems Richmond	Temperature Abuse	Nationwide
20 Sep 2017Device	CLASS II	Cell Marque, PAX8 (MRQ-50 Mab.) recalled by Leica Biosystems Richmond	Leica Biosystems Richmond	Temperature Abuse	Nationwide
29 Jun 2016Device	CLASS III	CytoVision Image Analysis and Capture System recalled	Leica Biosystems Richmond	Other	Nationwide
22 Jun 2016Device	CLASS III	Ariol is an automated scanning microscope and image analysis system recalled	Leica Biosystems Richmond	Device Malfunction	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.