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DeRoyal Industries Recalls
226 recalls on record · July 25, 2012 to June 10, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal TOTAL KNEE PACK, REF 89-9300.08
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal BIOPSY PACK, REF 89-9270.05
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal BIOPSY PACK, REF 89-9270.04
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal NEURO PACK, REF 89-9253.09
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal NEURO PACK, REF 89-9253.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal FOOT PACK, REF 89-9252.08
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal FOOT PACK, REF 89-9252.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal FOOT PACK, REF 89-9252.06
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal MAJOR ORTHO PACK, REF 89-9250.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal BASIC EYE PACK, REF 89-9233.08
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal TOTAL HIP PACK, REF 89-9113.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal TOTAL HIP PACK, REF 89-9113.06
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal LAMINECTOMY SPINAL FUSION PACK, REF 89-9105.10
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal LAMINECTOMY SPINAL FUSION PACK, REF 89-9105.09
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal LAMINECTOMY SPINAL FUSION PACK, REF 89-9105.08
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal KIT HEART B PACK, REF 89-9042.08
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal KIT HEART B PACK, REF 89-9042.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal KIT EXTREMITY PACK, REF 89-8869.09
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal KIT TOTAL HIP, REF 89-8861.07
Hazard: DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal TLIF PACK, REF 89-8780.04
Hazard: DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal ACDF PACK, REF 89-8779.03
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal SHOULDER ARTHROSCOPY PACK, REF 89-8777.04
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal EYE PACK, REF 89-8756.03
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls GEO-MED BIOPSY TRAY, REF 89-8753.01
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal PORT PACK PGYBK, REF 89-8748.05
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls GEO-MED PODIATRY PACK PGYBK, REF 89-8700.02
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls GEO-MED PODIATRY PACK PGYBK, REF 89-8700.01
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal BASIC PACK, REF 89-8633.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal CUSTOM NEURO PACK, REF 89-8392.10
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal CUSTOM NEURO PACK, REF 89-8392.09
Hazard: DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.