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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

39,519 recalled products

14,800 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

Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C PACEMAKER PK DYNJT3454 PACEMAKER/ICD PACK DYNJ33822L PAD OPEN HEART DYNJ900962O PEDIATRIC OPEN HEART DYNJ54238L DYNJT6766 STAZ BASIC VASCULAR DYNJ909794C VASCULAR ACCESS KIT CVI5323A VASCULAR CDS CDS983040M

Z-2418-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX PI CVC 7F, 3L, 20CM BUNDLE ECVC6915A ECVC6985B

Z-2439-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D DYNJ67197G DYNJ85197A DYNJT4007 BASIC ACCESS PACK-LF DYNJ36698B BASIC BACK TRAY DYNJ89037 BASIC PEDI PACK-LF DYNJ0171446I DYNJ0171446J BASIC SPINE DYNJ910915A BREAST PACK DYNJ87587A BREAST PLASTIC PACK DYNJ84482C C SECTION DYNJ49172I CAROTID ENDARTERECTOMY PACK DYNJ48013L CENTRAL LINE PACK-LF DYNJ0220136S CERVICAL FUSION DYNJ908135B CERVICAL SPINE PACK DYNJ53044G C-SECTION DYNJ909099F DAVINCI PROSTATE PACK DYNJ61711C DEPAUL FOOT & ANKLE-LF DYNJ20010L DIEP PACK DYNJ64964J DYNJ43210K DYNJ61787F DYNJ87065 EAR CUSTOM PACK DYNJ82564A ENT FREE FLAP PACK SAFETY DYNJ54720D EP PACEMAKER SAFETY #1 DYNJ54722F EPCH EXTREMITY PACK DYNJ83095B EXTREMITY PACK DYNJ32934F EXTREMITY PACK-LF DYNJ68935B FISTULA PACK DYNJ66502B GENDER AFFIRMING SURGERY DYNJ66252F GYN LAPAROSCOPY PACK AHSC DYNJT8381 HAND PACK WATCHMAKER-LF DYNJ34580D HEAD & NECK PACK-LF DYNJ0282388T DYNJ88308 HIP SCOPE DYNJ907120D KNEE ARTHRO PACK DYNJ58404F KNEE ARTHROSCOPY PACK DYNJ84740A LAMI OVERHEAD PACK DYNJ46531Q LAMINECTOMY NEURO MPH DYNJT5271 LAMINECTOMY PACK DYNJ68785D LAP APPY PACK DYNJT6005 LAP CHOLE PACK DYNJ82087A LEVY PACK DYNJ83939C MAJOR LAP VCH DYNJ39217P MAJOR NEURO PACK-LF DYNJ0578916AA MAJOR PACK DYNJ58528J MINOR GEN PACK DYNJ61661B MINOR LAPAROTOMY PACK-LF DYNJ0753436P MINOR PACK DYNJ54968B NEURO PACK DYNJ67628D NEURO SHUNT PACK-LF DYNJ0578815W OMFS PACK DYNJ54400C OPEN HEART PACK DYNJT5008 OPEN HEART-LF DYNJ48260F OPEN LAPAROTOMY PACK DYNJ39247I DYNJ39247J PACEMAKER PACK DYNJ31461I DYNJ61411C PACK,ORTHO FLIP DYNJ65471B PED OPEN HEART PACK DYNJ45373G PLASTIC PACK DYNJ82495D PLASTICS PK - NO SYR DYNJ62433F PODIATRY PACK OP7809M PPE BUNDLE KIT DT13351A PROSTATE ROBOTIC PACK DYNJ84120C RADIAL ART LINE INSERTION ARTNC234 ROBOTIC GENERAL WHH DYNJT5376 ROBOTIC PACK DYNJ47978G RR-SPINE PACK DYNJ62643B SHOULDER ARTH PACK DYNJ58410D SHOULDER ARTHROSCOPY PACK DYNJ54477C DYNJT8391 SHOULDER PACK DYNJ61052B DYNJT3266 SHOULDER PACK-LF DYNJ0122428K PHS656414I SPINE PACK DYNJ64949C DYNJ83649B SPINE SHOULDER PACK DYNJ47104D STERILE ACCESS KIT DYNDA2664 TOTAL KNEE PACK DYNJ84741B TUBAL PACK DYNJ68253F UNIVERSAL PACK DYNJ83246B VA TAMPA GENERAL ROBOTIC PACK DYNJT6993 W.C. MINOR LAPAROTOMY PK-LF DYNJ0509186J ZALE OTOLOGY CDS CDS983181G

Z-2441-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K

Z-2435-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS CATHETER MAINTENANCE KIT DT17570 DIALYSIS DRESSING CHANGE KIT DT21370B DRESSING CHANGE TRAY - GOLD DT21115B PORT DRESSING CHANGE KIT DYNDC2815A

Z-2437-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662

Z-2425-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B

Z-2442-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C

Z-2419-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D C-SECTION DYNJ905094B C-SECTION RECOVERY #2 CDS820091P

Z-2446-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F

Z-2429-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A

Z-2440-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L

Z-2420-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C

Z-2432-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D

Z-2427-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M

Z-2430-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G

Z-2417-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A CVC/PICC/MIDLINE DRESSING CHANGE KIT EBSI1057A DIALYSIS DRESSING CHANGE EBSI1498 EBSI CVC DRESSING CHANGE KIT EBSI1585 PICC DRESSING CHANGE TRAY EBSI1621 PORT ACCESS KIT EBSI1837

Z-2438-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: WT LAVH PACK DYNJ46609F

Z-2433-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A

Z-2416-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process control

Device enforcement product

Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887 DYNJT6876 GYN ROBOTIC CDS CDS984228K GYN ROBOTICS DYNJ911843 KIT LABOR DELIVERY TUBAL LIGAT DYKMBNDL165C ROBOTIC LAP CHOLE CDS CDS985442J ROBOTIC PACK DYNJ84725B DYNJ910594B ROBOTIC SURGERY PACK DYNJ53711B ROBOTICS PACK DYNJ83622C UOFL GYN LAPAROSCOPY DYNJ909322B WMC ROBOTIC PACK - LF DYNJ902583O

Z-2431-2026 · initiated April 27, 2026

Sourced
Recalling firm
Medline Industries, LP
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98951
Review official root-cause evidence and provenance

Official device-enrichment wording

Process 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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