Deroyal Industries, Inc. Lafollette recalls

Deroyal Industries, Inc. Lafollette has 12 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 6 Oct 2021. The most frequent reason is particulate matter.

Total recalls12since 2020
Last 12 months0reported
Class I18% of total
Ongoing0latest 6 Oct 2021

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 8%Class II 11 92%Class III 0 0%

Why deroyal industries, inc. lafollette is recalled

By year

All deroyal industries, inc. lafollette recalls, newest first

12 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IDeRoyal Procedure Packs containing Smiths Medical Normoflo recalledDeroyal Industries, Inc. LafolletteOtherFL, SC
DeviceCLASS IITeleflex Pilling Aortic Punch Sterile recalledDeroyal Industries, Inc. LafolletteSterilityNationwide
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI
DeviceCLASS IIDeRoyal Sterile Custom Kits containing Cardinal Health Gowns recalledDeroyal Industries, Inc. LafolletteParticulate MatterNJ, RI

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.