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Recall Observatory FDA recall evidence

Official device enrichment

Separate sourced root-cause wording from missing evidence.

This laboratory joins device enforcement products to public FDA device-enrichment records through documented exact identifiers. It preserves official wording and never turns an absent or conflicting join into a conclusion.

Four explicit evidence outcomes

What each state means

Global device-product counts

Sourced 32,075 products
At least one exact joined official device-enrichment row contains root-cause wording. The wording is preserved as an official fact, not an app conclusion.
? Unknown 7,441 products
An exact joined enrichment record exists, but none supplies supported root-cause wording. This does not mean FDA reported that the cause is unknown.
Unavailable 3 products
No public enrichment row could be joined through the supported exact identifiers, or the enrichment source itself was unavailable. This is not evidence of no root cause.
Ambiguous 0 products
Official identifier candidates conflict. Recall Observatory preserves the conflict and does not select a candidate or synthesize root-cause wording.

Coverage and provenance

Device sources represented

  • Device enrichment openFDA Device Recall · event_date_initiated coverage June 01, 1997–June 30, 2026 Official source · published July 16, 2026 07:05
  • Enforcement openFDA Device Enforcement · report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval. Official source · published July 16, 2026 07:03

Enforcement bounds use FDA report dates; device-enrichment bounds use FDA event_date_initiated. A product's recall-initiation date can precede enforcement report-date coverage.

Inspect corpus status

Exact official wording

Root-cause wording register

40 distinct wordings

Counts use distinct recalled products and exact recall events. Wording is grouped only by byte-for-byte database equality; similar phrases are not normalized, merged, ranked, or interpreted as equivalent causes.

Exact official device root-cause wording counts
Official root-cause wording Recalled products Exact events
Device Design
5,544 2,055
Process control
4,983 1,836
Nonconforming Material/Component
4,049 1,363
Software design
2,469 1,529
Packaging
1,376 150
Component design/selection
1,096 440
Other
984 377
No Marketing Application
941 214
Packaging process control
846 256
Process change control
807 277
Error in labeling
790 298
Process design
790 322
Employee error
749 410
Package design/selection
636 117
Labeling design
631 223
Equipment maintenance
505 126
Labeling Change Control
485 268
Material/Component Contamination
423 165
Labeling mix-ups
401 260
Component change control
391 154
Use error
316 142
Mixed-up of materials/components
290 180
Radiation Control for Health and Safety Act
274 181
Storage
270 42
Vendor change control
258 66
Packaging change control
255 72
Labeling False and Misleading
253 116
Software Design Change
209 145
Environmental control
186 36
Software change control
159 89
Incorrect or no expiration date
144 59
Software Manufacturing/Software Deployment
137 84
Software design (manufacturing process)
100 62
Reprocessing Controls
88 28
Manufacturing material removal
82 21
Software in the Use Environment
82 60
Release of Material/Component prior to receiving test results
40 28
Finished device change control
26 15
PMA
6 3
Counterfeit
4 4

Current device enforcement corpus

32,075 recalled products

12,273 exact events

Clear

The selected filter changes this product ledger and its product/event summary only. The four-state overview and exact-wording register remain global corpus context.

Device enforcement product

eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151

Z-1733-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

Z-1646-2026 · initiated March 02, 2026

Sourced
Recalling firm
Philips Respironics, Inc.
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98540
Review official root-cause evidence and provenance

Official device-enrichment wording

Software design

Device enforcement product

eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152

Z-1734-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.

Z-1647-2026 · initiated March 02, 2026

Sourced
Recalling firm
Philips Respironics, Inc.
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98540
Review official root-cause evidence and provenance

Official device-enrichment wording

Software design

Device enforcement product

Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

Z-1648-2026 · initiated March 02, 2026

Sourced
Recalling firm
Philips Respironics, Inc.
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98540
Review official root-cause evidence and provenance

Official device-enrichment wording

Software design

Device enforcement product

Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.

Z-1649-2026 · initiated March 02, 2026

Sourced
Recalling firm
Philips Respironics, Inc.
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98540
Review official root-cause evidence and provenance

Official device-enrichment wording

Software design

Device enforcement product

eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149

Z-1731-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150

Z-1732-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159

Z-1738-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157

Z-1736-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158

Z-1737-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

Z-1735-2026 · initiated March 02, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98513
Review official root-cause evidence and provenance

Official device-enrichment wording

Software change control

Device enforcement product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK DYNJ38587A, DYNJ38587B BIOPSY/DRAINAGE TRAY-LF DYNJ30078D W LINQ PACK DYNJ59108B

Z-1879-2026 · initiated February 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98601
Review official root-cause evidence and provenance

Official device-enrichment wording

Component change control

Device enforcement product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ909398A ROBOTIC PACK DYNJ908706D

Z-1885-2026 · initiated February 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98601
Review official root-cause evidence and provenance

Official device-enrichment wording

Component change control

Device enforcement product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BASIC CL PACK-LF DYNJ87052 BASIC PACK DYNJ83976 BASIC SET UP PACK DYNJ80700 CORONARY ANGIOGRAPHY PACK (N) DYNJ42136B CSTM ANGIO KIT - S VASC1109 CV PACK DYNJ46301C DR F PACK DYNJ41253B ENSEMBLE HEMORROIDES DYNJ56311A G TAVR PACK DYNJ61006 IR MINOR PACK DYNJ44139C MAJOR PLUS PACK DYNJ905160N MAXIMUM BARRIER BUNDLE PACK DYNJ35216C PCI PACK TBRHSC-LF DYNJ41941D PERC PACK-LF DYNJ0774759P PERIPHERAL ANGIOGRAPHY PK DYNJ42094B PROCEDURE PACK DYNJ55063B PTCA PACK DYNJ55359B ROBOTIC PACK DYNJ908706C SPECIAL PROCEDURES TRAY DYNJ41174A SYRINGE WIRE KIT SANFORD SAMPC0644 WPH EP PACK DYNJ62745 X-RAY PACK DYNJ44295G

Z-1883-2026 · initiated February 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98601
Review official root-cause evidence and provenance

Official device-enrichment wording

Component change control

Device enforcement product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BARIATRIC DYNJ905153M, DYNJ905153N GENERAL LAPAROSCOPY PACK DYNJ81602 LAPAROSCOPY DYNJ905157K, DYNJ905157L LAPAROTOMY PACK DYNJ46675G MAJOR LITHOTOMY PACK DYNJ81607 MAJOR PLUS PACK DYNJ905160O MINOR GENERAL PACK DYNJ81599

Z-1881-2026 · initiated February 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98601
Review official root-cause evidence and provenance

Official device-enrichment wording

Component change control

Device enforcement product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADD A ENDOVASCULAR PACK-LF DYNJ0429339L, DYNJ0429339M ANGIO ARTERIOGRAM PACK-LF DYNJ0774026K ANGIO KIT PACK DYNJ83746B ANGIO TRAY NO LIDO DYNJ85557A ANGIOGRAPHY PACK II DYNJ17218S, DYNJ17218T ARTERIOGRAM NEURO PACK-LF DYNJ0842499L ARTERIOGRAM PACK-LF DYNJ0842478M CARDIAC CATH II PK DYNJ21259O CARDIAC CATH PACK DYNJ68653D CATH LAB ANGIOGRAPHY PACK DYNJ50779G CATH LAB-LF DYNJ51423G CRANIOTOMY PACK-LF DYNJ0101292I DEEP BRAIN STIMULATION PACK DYNJ0842793I ENDO VASCULAR MINOR DYNJ87263 GENERAL ENDO PACK-LF DYNJ0842873L LEFT HEART DYNJ45984J LIPO PACK DYNJ87218 MAA Y90 TRAY DYNJ82191D MAIN OR CATH LAB DYNJ61373B MINIMALLY INVASIVE PACK-LF DYNJ0843063M NEURO CERVICAL PACK DYNJ0101287M NEURO RADIOLOGY RICHMOND DYNJ68365F NEURO VP SHUNT PACK-LF DYNJ0843121L NON-VASCULAR PACK DYNJ56386C, DYNJ56386D OR ANGIOGRAM PACK-LF DYNJ83656A, DYNJ83656B OR RADIOLOGY PACK DYNJ62747A PERCUTANEOUS ARTERIAL CATH PK DYNJ30551J PERIPHERAL ARTERIOGRAM RAD DYNJ61383C PICC ABSCESS PACK-LF DYNJ0774005I PICC TRAY DYNJ30554I PODIATRY PACK DYNJ46333G POSTERIOR SPINE PACK-LF DYNJ0843339P RRMC ANGIO PACK DYNJ36338D SPECIAL PROCEDURE PACK DYNJ88258 VASCULAR ACCESS PACK-LF DYNJ0101291G VASCULAR HYBRID DYNJ57543K VASCULAR PACK DYNJ82220D VISCERAL ANGIOGRAM PACK-LF DYNJ0429121M WPH EP PACK DYNJ62745A

Z-1890-2026 · initiated February 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98601
Review official root-cause evidence and provenance

Official device-enrichment wording

Component change control

Device enforcement product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EXTREMITY PACK DYNJ34846C HAND PACK DYNJ83218A, DYNJ85396 LAMINECTOMY DYNJ905156R MAJOR EXTREMITY DYNJ905159L, DYNJ905159M MAJOR EXTREMITY PACK DYNJ69926A PODIATRY PACK DYNJ41250B

Z-1887-2026 · initiated February 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98601
Review official root-cause evidence and provenance

Official device-enrichment wording

Component change control

Device enforcement product

Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-CPLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tissue with moderate hemostasis, little charring, and a thin zone of necrosis. Component: No

Z-1694-2026 · initiated February 27, 2026

Sourced
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98422
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes TAVR PACK DYNJ69246B ABDOMINAL VASCULAR-LF DYNJ905291D ANGIOGRAPHIC PACK DYNJ86769 AORTAGRAM PACK DYNJ26783D AV FISTULA PACK CHS-LF DYNJ35615G AV SHUNT PACK-LF DYNJ0842516G CATHETER PACK DYNJ61926 EP DRAPE PACK-LF DYNJ47645C EP PACK DYNJ47782G EPS ACCESSORY PACK DYNJT2201S H CLINIC VASCULAR PK DYNJ33415A HEART FAILURE PACK DYNJ64877B HYBRID PACK DYNJ65925D INTERVENTIONAL RAD PACK DYNJ44100M INTERVENTIONAL RADIOLOGY PK-LF DYNJ0516014AG MV-PACEMAKER PACK-LF DYNJ41556F NEURO RADIOLOGY RICHMOND DYNJ68365D OR HYBRID-M DYNJ907758D, DYNJ907758F PACEMAKER DYNJ907960C PACEMAKER PACK DYNJ42557B DYNJ61411 DYNJ61411A DYNJ61411B DYNJ80160 PACER PACK DYNJ40952B PERIPHERAL ARTERIOGRAM RAD DYNJ61383B RADIOLOGY PACK DYNJ54762D TAVR PACK DYNJ55338B DYNJ69246A VASCULAR ACCESS TRAY DYNJ52606F VASCULAR TRAY DYNJ49802C VEIN PACK DYNJ57512 DYNJ58063 DYNJ84953

Z-1878-2026 · initiated February 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98601
Review official root-cause evidence and provenance

Official device-enrichment wording

Component change control

Evidence boundary: this page reports official device-enrichment wording and exact join outcomes. It does not infer a root cause, merge similar phrases, or treat missing enrichment as evidence of no root cause. Review the full methodology

Field note

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