Fisher Diagnostics recalls

Fisher Diagnostics has 4 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 9 Apr 2025. 2 are still ongoing. The most frequent reason is potency & assay.

Total recalls4since 2017

Last 12 months0reported

Class I00% of total

Ongoing2latest 9 Apr 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 2Apr 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 4 100%Class III 0 0%

Why fisher diagnostics is recalled

Potency & Assay4100%

Product types

Test Kits & Diagnostics4100%

By year

2025250%
2017250%

Ongoing fisher diagnostics recalls

2 active

Reported	Class	Recall	Company	Reason	Where
9 Apr 2025Device	CLASS II	Pacific Hemostasis Thromboplastin-D Used recalled by Fisher Diagnostics	Fisher Diagnostics	Potency & Assay	PA
9 Apr 2025Device	CLASS II	Pacific Hemostasis Thromboplastin-D Used recalled by Fisher Diagnostics	Fisher Diagnostics	Potency & Assay	PA

All fisher diagnostics recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
9 Apr 2025Device	CLASS II	Pacific Hemostasis Thromboplastin-D Used recalled by Fisher Diagnostics	Fisher Diagnostics	Potency & Assay	PA
9 Apr 2025Device	CLASS II	Pacific Hemostasis Thromboplastin-D Used recalled by Fisher Diagnostics	Fisher Diagnostics	Potency & Assay	PA
2 Aug 2017Device	CLASS II	Pacific Hemostasis FDP Latex Reagent recalled by Fisher Diagnostics	Fisher Diagnostics	Potency & Assay	Nationwide
2 Aug 2017Device	CLASS II	Pacific Hemostasis FDP (Fibrinogen Degradation Products) recalled	Fisher Diagnostics	Potency & Assay	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.