Core noun
Device recall evidence
Joined enrichment rows that support device recall linkage and root-cause wording.
Indexed record set
39,516 evidence rows
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- Evidence
- device-recall:cfres:210297
- Product
- Abbott Alinity m STI AMP Kit, used with the Alinity m System, product codes: a) REF 09N17-095; b) REF 09N17-090; c) REF 09N17-091;
- Join
- Official recall number ·
Z-0234-2025 - Root cause
- Device Design
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- Evidence
- device-recall:cfres:210277
- Product
- medex TranStar 60in (152cm) Single Monitoring Kit 10/EA, Product Code REF MX9504T
- Join
- Official recall number ·
Z-0191-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210213
- Product
- Quest Spectrum 3 Fluorescent Imaging System Model/Catalog Number: ART-SYS-0029, ART-SYS-0030 The Quest Spectrum3 is a fluorescent imaging system used in capturing and viewing fluorescent images for the visual assessment of blood flow for the evaluation of tissue perfusion, and related tissue-transfer circulation in tissue and free flaps used during plastic and reconstructive surgeries.
- Join
- Official recall number ·
Z-0232-2025 - Root cause
- Component design/selection
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- Evidence
- device-recall:cfres:210291
- Product
- medex TranStar MONITORING SET W/SAMPLING PORT 10/EA, Product Code REF MXG300260
- Join
- Official recall number ·
Z-0204-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210173
- Product
- Centurion OB TRAY, REF MNS13965A; medical procedure convenience kit
- Join
- Official recall number ·
Z-0151-2025 - Root cause
- Under Investigation by firm
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- Evidence
- device-recall:cfres:210283
- Product
- medex TranStar KIDS KIT 19IN. CLOSED BLOOD SAMPLE KIT with 30cc/hr Flush Device 10/EA, Product Code REF MX9543
- Join
- Official recall number ·
Z-0197-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210177
- Product
- Medline brand, medical procedure convenience kits, labeled as: a) RADIOLOGY LP TRAY, REF DYNDH1609; b) CARDIAC CATH PACK-LF, REF DYNJ19010I; c) SUPPLEMENTAL NEURO ANGIO PK, REF DYNJ29207; d) ANGIO PACK, REF DYNJ43661C; e) LEFT HEART CATH TEGH-LF, REF DYNJ46746C; f) LFT HRT CATH RADIAL ACCESS-LF, REF DYNJ47667C; g) IR ARM PACK, REF DYNJ50712D; h) IR PACK, REF DYNJ67324; i) PL. CATHETERISME CARDIAQUE, REF HCT093J
- Join
- Official recall number ·
Z-0155-2025 - Root cause
- Under Investigation by firm
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- Evidence
- device-recall:cfres:209684
- Product
- smiths medical portex, Y' PIECE 15MM, REF 100/276/000
- Join
- Official recall number ·
Z-0145-2025 - Root cause
- Packaging process control
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- Evidence
- device-recall:cfres:210171
- Product
- Centurion EP LAB INSTRUMENT KIT, REF MNS10480; medical procedure convenience kit
- Join
- Official recall number ·
Z-0149-2025 - Root cause
- Under Investigation by firm
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- Evidence
- device-recall:cfres:210202
- Product
- Medline EYE PACK, REF LYN036EPESB; medical procedure convenience kit
- Join
- Official recall number ·
Z-0180-2025 - Root cause
- Under Investigation by firm
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- Evidence
- device-recall:cfres:210281
- Product
- medex TranStar DPT w/Two Stopcocks 10/EA, Product Code REF MX950X2SC
- Join
- Official recall number ·
Z-0195-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210516
- Product
- Halyard EXTREMITY PACK - Medical convenience kits Model Number: MMOK009-03
- Join
- Official recall number ·
Z-0416-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210633
- Product
- Halyard PACK, MINOR - Medical convenience kits Model Number: VMED018-02
- Join
- Official recall number ·
Z-0452-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210412
- Product
- MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 720001F2
- Join
- Official recall number ·
Z-0459-2025 - Root cause
- Component design/selection
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- Evidence
- device-recall:cfres:210498
- Product
- Halyard ABDOMINAL PROCEDURE - Medical convenience kits Model Number: GRAN015-06
- Join
- Official recall number ·
Z-0399-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210521
- Product
- Halyard HEART CATH LAB PK, STRL F G - Medical convenience kits Model Number: MSBM003-03
- Join
- Official recall number ·
Z-0418-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210660
- Product
- CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-1.
- Join
- Official recall number ·
Z-0478-2025 - Root cause
- Nonconforming Material/Component
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- Evidence
- device-recall:cfres:210601
- Product
- Halyard SAMMC ANGIOGRAPHY - Medical convenience kits Model Number: SAMM066-15
- Join
- Official recall number ·
Z-0430-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:210831
- Product
- URINALYSIS KIT 4, SKU DYLAB1021; Component No. 503581
- Join
- Official recall number ·
Z-0357-2025 - Root cause
- Under Investigation by firm
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- Evidence
- device-recall:cfres:210488
- Product
- Halyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-03
- Join
- Official recall number ·
Z-0397-2025 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:210614
- Product
- Halyard CATH LAB PACK - Medical convenience kits Model Number: VANW016-05
- Join
- Official recall number ·
Z-0437-2025 - Root cause
- Process control
-
- Evidence
- device-recall:cfres:210473
- Product
- Halyard IR BIOPSY PACK - Medical convenience kits Model Number: AVMD019-01
- Join
- Official recall number ·
Z-0384-2025 - Root cause
- Process control
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- Evidence
- device-recall:cfres:209236
- Product
- KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the function of the upper limb on one side of the body.
- Join
- Official recall number ·
Z-0049-2025 - Root cause
- Device Design
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- Evidence
- device-recall:cfres:210080
- Product
- basixTOUCH Inflation Device, REF: IN8130/JPC, IN8152/C, IN8302/C, IN8352/C, IN8802/C, IN8130/C, IN8130/C
- Join
- Official recall number ·
Z-0072-2025 - Root cause
- Packaging process control
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- Evidence
- device-recall:cfres:210028
- Product
- Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006, MON-000006-RFB.
- Join
- Official recall number ·
Z-0051-2025 - Root cause
- Device Design