PlainRecalls

DeRoyal Industries Inc

153 recalls on record · Latest: Feb 26, 2025

DeRoyal Industries Inc Recall Insight

DeRoyal Industries Inc appears on 153 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.182% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Feb 26, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Dec 21, 2022 to Dec 21, 2022.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Dec 21, 2022

DeRoyal CUSTOM NEURO PACK, REF 89-7353.17

FDA Devices Moderate Dec 21, 2022

DeRoyal EMERGENT TRAUMA PACK, REF 89-9453.14

FDA Devices Moderate Dec 21, 2022

DeRoyal LAMINECTOMY SPINAL FUSION PACK, REF 89-9105.08

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-9241.04

FDA Devices Moderate Dec 21, 2022

DeRoyal CRANI PACK, REF 89-10202.03

FDA Devices Moderate Dec 21, 2022

DeRoyal LAPINECTOMY PACK, REF 89-7198.11

FDA Devices Moderate Dec 21, 2022

DeRoyal TOTAL HIP PACK, REF 89-9113.06

FDA Devices Moderate Dec 21, 2022

DeRoyal TOTAL HIP PACK, REF 89-9113.07

FDA Devices Moderate Dec 21, 2022

DeRoyal PACEMAKER ICD PACK, REF 89-10902.01

FDA Devices Moderate Dec 21, 2022

DeRoyal SPINE PACK, REF 89-8361.08

FDA Devices Moderate Dec 21, 2022

DeRoyal KIT TOTAL HIP, REF 89-8861.07

FDA Devices Moderate Dec 21, 2022

DeRoyal CRANI PACK, REF 89-10202.05

FDA Devices Moderate Dec 21, 2022

DeRoyal LUMBAR DISC PACK, REF 89-10590.02

FDA Devices Moderate Dec 21, 2022

DeRoyal SPINE PACK, REF 89-8361.09

FDA Devices Moderate Dec 21, 2022

DeRoyal UNIVERSAL PACK, REF 89-9558.03

FDA Devices Moderate Dec 21, 2022

DeRoyal POSTERIOR LAMI MICRODISC PACK, REF 89-10059.02

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-9241.03

FDA Devices Moderate Dec 21, 2022

DeRoyal POSTERIOR LUMBAR FUSION PACK, REF 89-10060.02

FDA Devices Moderate Dec 21, 2022

DeRoyal BIOPSY PACKPACK, REF 89-9756.05

FDA Devices Moderate Dec 21, 2022

DeRoyal LUMBAR DISC PACK, REF 89-10605.02

FDA Devices Moderate Dec 21, 2022

DeRoyal EMERGENT TRAUMA PACK, REF 89-9453.13

FDA Devices Moderate Dec 21, 2022

DeRoyal PORT PACK PGYBK, REF 89-8748.05

FDA Devices Moderate Dec 21, 2022

GEO-MED KNEE ARTHROSCOPY PACK, REF 89-5795.07

FDA Devices Moderate Dec 21, 2022

DeRoyal LUMBAR FUSION PACK, REF 89-10211.05

FDA Devices Moderate Dec 21, 2022

DeRoyal LAMI/CRANI PACK, REF 89-10787.01

FDA Devices Moderate Dec 21, 2022

DeRoyal SPINAL FUSION PACK, REF 89-7515.13

FDA Devices Moderate Dec 21, 2022

DeRoyal HEART PACK, REF 89-8351.12

FDA Devices Moderate Dec 21, 2022

DeRoyal CRANI PACK, REF 89-10242.02

FDA Devices Moderate Dec 21, 2022

DeRoyal BASIC NEURO PACK, REF 89-7523.15

FDA Devices Moderate Dec 21, 2022

DeRoyal SHOULDER ARTHOSCOPY PACK, REF 89-9946.04

FDA Devices Moderate Dec 21, 2022

GEO-MED UPPER EXTERMITY PACK, REF 89-8253.02

FDA Devices Moderate Dec 21, 2022

GEO-MED BIOPSY TRAY, REF 89-8753.01

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-10040.01

FDA Devices Moderate Dec 21, 2022

DeRoyal ANTERIOR APPROACH TOTAL HIP A&B PGYBK, REF 89-10612.01

FDA Devices Moderate Dec 21, 2022

DeRoyal TOTAL KNEE PACK A & B PACK, REF 89-6799.02

FDA Devices Moderate Dec 21, 2022

DeRoyal OPEN SHOULDER PROCEDURE PACK RF, REF 89-6629.09

FDA Devices Moderate Dec 21, 2022

DeRoyal GU PACK, REF 89-10665.03

FDA Devices Moderate Dec 21, 2022

DeRoyal BIOPSY PACK, REF 89-9739.05

FDA Devices Moderate Dec 21, 2022

DeRoyal ENDOVASCULAR TRACEPACK, REF 89-9350.03

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-8650.10

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-8859.08

FDA Devices Moderate Dec 21, 2022

DeRoyal CNRV SPINAL PACK, REF 89-10532.03

FDA Devices Moderate Dec 21, 2022

DeRoyal HEART PACK, REF 89-8351.13

FDA Devices Moderate Dec 21, 2022

DeRoyal BASIC NEURO PACK, REF 89-7523.16

FDA Devices Moderate Dec 21, 2022

DeRoyal ACDF PACK PGYBK A PACK / B PACK, REF 89-9997.06

FDA Devices Moderate Dec 21, 2022

GEO-MED CATARACT PACK, REF 89-5790.08

FDA Devices Moderate Dec 21, 2022

DeRoyal SHOULDER ARTHOSCOPY PACK, REF 89-10820.02

FDA Devices Moderate Dec 21, 2022

DeRoyal TLIF PACK, REF 89-8780.04

FDA Devices Moderate Dec 21, 2022

DeRoyal ACDF PACK, REF 89-8779.03

FDA Devices Moderate Dec 21, 2022

DeRoyal ORTHO SPINE BACK PACK, REF 89-7534.09

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds