Skip to content
Recalls · Brand

Leica Biosystems Richmond Inc. recalls

Every recall we track for Leica Biosystems Richmond Inc. — 7 in all, all from 2017 — plus the complaints and injury reports the public filed about them.

7recalls

Recalls per year, by danger level

Recalls from Leica Biosystems Richmond Inc. peaked in 2017 (7); 7 since 2017.

2017: 7 recalls — 7 lower risk720172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 0 recalls20212022: 0 recalls20222023: 0 recalls20232024: 0 recalls20242025: 0 recalls20252026 (to date): 0 recalls2026to date

All FDA recall records for Leica Biosystems Richmond Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Leica Biosystems Richmond Inc., by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700707
201800000
201900000
202000000
202100000
202200000
202300000
202400000
202500000
2026 (to date)00000

What to do if you have a recalled Leica Biosystems Richmond Inc. product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Leica Biosystems Richmond Inc. recalls

1 shown

Leica Biosystems Richmond Inc. recall questions

How many recalls has Leica Biosystems Richmond Inc. had?

7 recalls from Leica Biosystems Richmond Inc. are on record with U.S. safety agencies, from 2017.

What is the most recent Leica Biosystems Richmond Inc. recall?

Leica Biosystems Richmond Inc. recalls Cell Marque, PAX8 (MRQ-50 Mab.), 7 mL, REF PA0808, IVD, This antibody is intended for in vitro diagnostic (IVD) use., dated Jul 14, 2017. Every Leica Biosystems Richmond Inc. recall is listed on this page, newest first.

What should I do if I have a recalled Leica Biosystems Richmond Inc. product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Leica Biosystems Richmond Inc. recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.