Skip to content
Recall Observatory FDA recall evidence

Core noun

Device recall evidence

Joined enrichment rows that support device recall linkage and root-cause wording.

Indexed record set

39,516 evidence rows

Page 65 of 1581

Evidence Product Join Root cause
device-recall:cfres:197384 DeRoyal Tonsillectomy Tray, REF 89-10698.01 Official recall number · Z-0906-2023 Nonconforming Material/Component
device-recall:cfres:196854 STRADIS HEALTHCARE, Femoral, Vasc, Item No.686-142, Official recall number · Z-0553-2023 Packaging process control
device-recall:cfres:196929 DeRoyal SPINE PACK, REF 89-8361.10 Official recall number · Z-0615-2023 Nonconforming Material/Component
device-recall:cfres:196822 HENRY SCHEIN, BASIC EXTENDED PACK, Item No.570-2890 Official recall number · Z-0521-2023 Packaging process control
device-recall:cfres:196912 DeRoyal SPINAL FUSION PACK, REF 89-7515.14 Official recall number · Z-0598-2023 Nonconforming Material/Component
device-recall:cfres:196851 STRADIS HEALTHCARE, Endo Pack, Item No.682-509, Official recall number · Z-0550-2023 Packaging process control
device-recall:cfres:196960 DeRoyal TOTAL KNEE PACK, REF 89-9300.08 Official recall number · Z-0645-2023 Nonconforming Material/Component
device-recall:cfres:196793 Surgical room, SURGICAL PACK, Item No.40996WLS, oral surgery tray Official recall number · Z-0492-2023 Packaging process control
device-recall:cfres:196901 DeRoyal TRANS CANAL PACK, REF 89-7157.12 Official recall number · Z-0587-2023 Nonconforming Material/Component
device-recall:cfres:196981 DeRoyal SHOULDER ARTHOSCOPY PACK, REF 89-9946.04 Official recall number · Z-0666-2023 Nonconforming Material/Component
device-recall:cfres:196899 DeRoyal GU ROBOTIC PACK, REF 89-7063.12 Official recall number · Z-0585-2023 Nonconforming Material/Component
device-recall:cfres:196824 HENRY SCHEIN, PROCEDURE TRAY, Item No.570-2900, Official recall number · Z-0523-2023 Packaging process control
device-recall:cfres:196785 BASIC IMPLANT PACK, Item No. 40310SBI, oral surgery tray Official recall number · Z-0484-2023 Packaging process control
device-recall:cfres:196984 DeRoyal POSTERIOR LAMI MICRODISC PACK, REF 89-10059.02 Official recall number · Z-0669-2023 Nonconforming Material/Component
device-recall:cfres:197166 Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400F (IPN000306), cardiac pump Official recall number · Z-0445-2023 Pending
device-recall:cfres:196927 DeRoyal SPINE PACK, REF 89-8361.08 Official recall number · Z-0613-2023 Nonconforming Material/Component
device-recall:cfres:196827 HENRY SCHEIN, EXTREMITY PACK, Item No.570-2946 Official recall number · Z-0526-2023 Packaging process control
device-recall:cfres:197007 DeRoyal CMC POSTERIOR SPINE PACK, REF 89-10570.01 Official recall number · Z-0692-2023 Nonconforming Material/Component
device-recall:cfres:196522 Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT 2 IAPB, REF IAP-0400 (IPN000302), cardiac pump Official recall number · Z-0426-2023 Pending
device-recall:cfres:197006 DeRoyal CARDIAC LINEN PACK, REF 89-10543.02 Official recall number · Z-0691-2023 Nonconforming Material/Component
device-recall:cfres:196977 DeRoyal BIOPSY PACK, REF 89-9614.07 Official recall number · Z-0662-2023 Nonconforming Material/Component
device-recall:cfres:196843 STRADIS HEALTHCARE, Surgery PK, Item No.682-1728, Official recall number · Z-0542-2023 Packaging process control
device-recall:cfres:196874 DeRoyal MAJOR ORAL PACK RF, REF 89-3936.15 Official recall number · Z-0561-2023 Nonconforming Material/Component
device-recall:cfres:197232 DeRoyal CATARACT PACK, REF 89-10086.05 Official recall number · Z-0715-2023 Nonconforming Material/Component
device-recall:cfres:196917 DeRoyal EYE TRAY PGYBK, REF 89-7978.02 Official recall number · Z-0603-2023 Nonconforming Material/Component

Field note

Send feedback

We'll only use this to respond to your feedback.