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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 GU ROBOTIC PACK, REF 89-7063.12
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal LAPAROSCOPIC ROBOTIC TRAY, REF 89-7063.11
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal BREAST TRAY, REF 89-7033.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal CANNULTED HIP PACK, REF 89-6977.10
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal CANNULTED HIP PACK CSM, REF 89-6977.09
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 CATARACT PACK CSM, REF 89-6863
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 SHOULDER PACK, REF 89-6830.13
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls GEO-MED TOTAL KNEE PACK A & B, REF 89-6799.02
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls GEO-MED PLASTIC HAND PACK RF, REF 89-6667.10
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls GEO-MED PLASTIC HAND PACK RF, REF 89-6667.09
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal OPEN SHOULDER PROCEDURE PACK RF, REF 89-6629.09
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 OPEN SHOULDER PROCEDURE PACK RF, REF 89-6629.07
Hazard: XXX
December 21, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal SHOULDER ARTHORSCOPY PACK RF, REF 89-6628.09
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 GEO-MED OPTHALMOLOGY CSTM PCK, REF 89-6387.09
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 GEO-MED OPTHALMOLOGY CSTM PCK, REF 89-6387.08
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 GEO-MED PODIATRY PACK PGYBK, REF 89-6240.05
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 PICC LINE TRAY PGYBK, REF 89-6150.13
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 GEO-MED SHOULDER ARTHROSCOPY KNEE PACK, REF 89-5797.09
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 GEO-MED TOTAL KNEE PACK A & B PGYK, REF 89-5796.13
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 GEO-MED KNEE ARTHROSCOPY PACK, REF 89-5795.07
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 PEDI ORTHO PACK, REF 89-5323.20
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 EYE TRAY, REF 89-4957.08
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 EXTREMITY TRAY PGYBK, REF 89-4081.07
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 EYE PACK, REF 89-4051.09
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 MAJOR ORAL PACK RF, REF 89-3936.15
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 MINOR ORAL / ENT PACK, REF 89-2576.15
Hazard: DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
September 7, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
Hazard: Procedure packs contained a recalled product.
August 31, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal limb holders: (1) DeRoyal Limb Holder, Wrist, Fixed, Quick Release, REF M8124; (2) DeRoyal Limb Holder, Ankl
Hazard: The webbing strap was laced improperly through the teeth of the buckle allowing the webbing strap to slide and was, therefore, not secure.
April 13, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal DEXMED ACCESS CENTER TRAY, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl alcohol) swab
Hazard: A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products.
April 13, 2022Medical DevicesFDA
DeRoyal Industries Inc recalls DeRoyal Ultra/Mammo Tray, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl alcohol) swab, for pre
Hazard: A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products.