Core noun
Device recall evidence
Joined enrichment rows that support device recall linkage and root-cause wording.
Indexed record set
39,516 evidence rows
-
- Evidence
- device-recall:cfres:211337
- Product
- Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
- Join
- Official recall number ·
Z-0884-2025 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:211580
- Product
- Otological Ventilation Tube - T-Tube 9mm - Double - Silicone; Product Code: NZ3309-2;
- Join
- Official recall number ·
Z-0965-2025 - Root cause
- Device Design
-
- Evidence
- device-recall:cfres:206158
- Product
- NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
- Join
- Official recall number ·
Z-1264-2024 - Root cause
- Packaging
-
- Evidence
- device-recall:cfres:205944
- Product
- CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
- Join
- Official recall number ·
Z-1291-2024 - Root cause
- Under Investigation by firm
-
- Evidence
- device-recall:cfres:205971
- Product
- D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
- Join
- Official recall number ·
Z-1278-2024 - Root cause
- Device Design
-
- Evidence
- device-recall:cfres:206366
- Product
- Exactech Equinoxe REVERSE SHOULDER,46mm Humeral Liner, a) +0mm, Item number 320-46-00, b) +2.5mm, Item Number 320-46-03; Shoulder Arthroplasty
- Join
- Official recall number ·
Z-1424-2024 - Root cause
- Nonconforming Material/Component
-
- Evidence
- device-recall:cfres:206411
- Product
- Centurion kits: a) DENTAL INSTRUMENT KIT, Product Code DH760; b) STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125ST6; c) DENTAL INSTRUMENT KIT, Product Code DH760
- Join
- Official recall number ·
Z-1431-2024 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:206409
- Product
- Centurion STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125ST6
- Join
- Official recall number ·
Z-1429-2024 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:205717
- Product
- DISP.HASSON TROCAR 12/110MM, Product Code EK240SU. For use in laparoscopic procedures.
- Join
- Official recall number ·
Z-1247-2024 - Root cause
- Packaging change control
-
- Evidence
- device-recall:cfres:205711
- Product
- Centurion Kits, trays, and packs labeled as follows: EYE PREP KIT, REF ET1010
- Join
- Official recall number ·
Z-1131-2024 - Root cause
- Nonconforming Material/Component
-
- Evidence
- device-recall:cfres:205642
- Product
- Medline Kits, trays, and packs labeled as follows: a) BREAST PACK, REF DYNJ56344B; b) SEPTOPLASTY PACK WRO-LF, REF DYNJ62803
- Join
- Official recall number ·
Z-1109-2024 - Root cause
- Nonconforming Material/Component
-
- Evidence
- device-recall:cfres:205654
- Product
- Medline Kits, trays, and packs labeled as follows: a) BLOOD DRAW KIT, REF DYNDV2183A; b) LCPH LAB DRAW KIT, REF DYNDH1641A; c) LCPH LAB DRAW KIT, REF DYNDH1641AH; d) OB LAB COLLECTION KIT, REF DYNDH1719A;
- Join
- Official recall number ·
Z-1115-2024 - Root cause
- Nonconforming Material/Component
-
- Evidence
- device-recall:cfres:206596
- Product
- Ureteral dilator, REF RBD014
- Join
- Official recall number ·
Z-1463-2024 - Root cause
- Under Investigation by firm
-
- Evidence
- device-recall:cfres:206394
- Product
- Covidien Auto Suture" Structural Balloon Trocar, Product Number OMS-T10SB
- Join
- Official recall number ·
Z-1465-2024 - Root cause
- Labeling design
-
- Evidence
- device-recall:cfres:206506
- Product
- Mojo Non Vented Full Face Mask with Headgear, All Sizes
- Join
- Official recall number ·
Z-1352-2024 - Root cause
- Device Design
-
- Evidence
- device-recall:cfres:206558
- Product
- KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b, a) REF 0209P and b) REF 0209K, Quality control kit for culture media
- Join
- Official recall number ·
Z-1483-2024 - Root cause
- Use error
-
- Evidence
- device-recall:cfres:206462
- Product
- Hemostasis Probe, Model: CD-B622LA
- Join
- Official recall number ·
Z-1481-2024 - Root cause
- Employee error
-
- Evidence
- device-recall:cfres:206563
- Product
- Alinity i Anti-HCV Reagent Kit, List Number 08P0521
- Join
- Official recall number ·
Z-1480-2024 - Root cause
- Device Design
-
- Evidence
- device-recall:cfres:206513
- Product
- Karl Storz SE & CO. KG, REF 115400S, Optical Scissor, CE
- Join
- Official recall number ·
Z-1473-2024 - Root cause
- Under Investigation by firm
-
- Evidence
- device-recall:cfres:206392
- Product
- GeoMed Custom Tracecarts, REF Numbers: a) 53-1831 ORTHO TOTAL JOINT TRACECART, b) 53-1836 GENERAL SURGERY TRACECART
- Join
- Official recall number ·
Z-1382-2024 - Root cause
- Other
-
- Evidence
- device-recall:cfres:206181
- Product
- Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral access to the vascular system
- Join
- Official recall number ·
Z-1390-2024 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:206387
- Product
- SOLTIVE Premium SuperPulsed Laser (TFL-PLS )
- Join
- Official recall number ·
Z-1385-2024 - Root cause
- Under Investigation by firm
-
- Evidence
- device-recall:cfres:206454
- Product
- Centurion Manual surgical kits labeled as: a) STERILE S/B WIRE SCISSOR, Product Code 65140; b) SHARP/SHARP SCISSORS 41/2", Product Code 65840; c) STERILE WIRE CUTTER (WCS144), Product Code 66240; d) STERILE LISTER BANDAGE SCISSOR (LS122), Product Code 66855; e) STERILE UTILITY SHEARS (USH176), Product Code 67225; f) STERILE ANGLED BANDAGE SCISSOR (LIST55), Product Code TRI66670
- Join
- Official recall number ·
Z-1449-2024 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:206426
- Product
- Centurion hook kits labeled as: a) STERILE SKIN HOOK FINE (EA3975F), Product Code 66660; b) STERILE SMALL 2 PRONG SKIN HOOK (25754), Product Code 67105; c) STERILE NEWS TRACH HOOK(83300), Product Code 67810; d) STERILE LILLIE EAR HOOK DELICATE 7", Product Code I68655
- Join
- Official recall number ·
Z-1435-2024 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:205748
- Product
- RELAY PRO Thoracic Stent-Graft System, containing one endovascular stent-graft system, IFU, and patient tracking card, sterile: (a) Part number 28-M4-34-100-34U; (b) Part number 28-M4-30-095-30U; (c) Part number 28-M4-46-155-46U; (d) Part number 28-M4-32-155-32S; (e) Part number 28-M4-36-250-32S; (f) Part number 28-M4-38-145-34S; (g) Part number 28-M4-38-190-38S; (h) Part number 28-M4-44-105-44S; (i) Part number 28-N4-22-099-22S; (j) Part number 28-N4-22-159-22S; (k) Part number 28-N4-24-099-24S; (l) Part number 28-N4-28-204-24S (m) Part number 28-N4-30-164-30U; (n) Part number 28-N4-32-164-28S; (o) Part number 28-N4-34-154-34U; (p) Part number 28-N4-34-209-30S; (q) RELAY PRO Custom-Made Device, REF 28NC36N19038S2590, part number 28-CMP-3062-NC; and (r) RELAY PRO Custom-Made Device, REF 28MC36A17536S2390, part number 28-CMP-3074-MC;
- Join
- Official recall number ·
Z-1383-2024 - Root cause
- Under Investigation by firm