Medical DeviceDec 21, 2022
DeRoyal SPINAL FUSION PACK, REF 89-7515.12 recall — FDA Z-0596-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Recall history in this database
Classification mix: Class II: 75, Class I: 3, Class III: 2.
Medical DeviceDec 21, 2022
DeRoyal KIT TOTAL HIP, REF 89-8861.07 recall — FDA Z-0627-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal SPINE PACK, REF 89-8361.09 recall — FDA Z-0614-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal Industries GEO-MED KNEE ARTHROSCOPY PACK, REF 89-5795.07 recall — FDA Z-0566-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal SPINAL FUSION PACK, REF 89-7515.13 recall — FDA Z-0597-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal HEART PACK, REF 89-8351.12 recall — FDA Z-0609-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal OPEN SHOULDER PROCEDURE PACK RF, REF 89-6629.09 recall — FDA Z-0575-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal TLIF PACK, REF 89-8780.04 recall — FDA Z-0626-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal PICC LINE TRAY PGYBK, REF 89-6150.13 recall — FDA Z-0569-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal CANNULTED HIP PACK CSM, REF 89-6977.09 recall — FDA Z-0581-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal SHOULDER ARTHORSCOPY PACK RF, REF 89-6628.09 recall — FDA Z-0573-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal Industries GEO-MED LOWER EXTERMITY PACK, REF 89-8252.02 recall — FDA Z-0604-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal Industries GEO-MED SHOULDER ARTHROSCOPY KNEE PACK, REF 89-5797.09 recall — FDA Z-0568-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal EXTREMITY TRAY PGYBK, REF 89-4081.07 recall — FDA Z-0563-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal EYE TRAY PGYBK, REF 89-7978.02 recall — FDA Z-0603-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal CATARACT PACK, REF 89-7135.10 recall — FDA Z-0586-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal SPINE PACK, REF 89-8361.10 recall — FDA Z-0615-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal BASIC NEURO PACK, REF 89-7258.12 recall — FDA Z-0591-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal Industries GEO-MED OPTHALMOLOGY CSTM PCK, REF 89-6387.08 recall — FDA Z-0571-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal SPINAL FUSION PACK, REF 89-7515.14 recall — FDA Z-0598-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal ENDOVENOUS PACK, REF 89-7762.05 recall — FDA Z-0602-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal CUSTOM NEURO PACK, REF 89-8392.09 recall — FDA Z-0616-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal BASIC NEURO PACK, REF 89-7258.13 recall — FDA Z-0592-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal EYE PACK, REF 89-4051.09 recall — FDA Z-0562-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies DeRoyal Industries Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.