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 19, 2026 02:15
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.
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
7,441 recalled products
2,526 exact events
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
Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro Diagnostic test kit for the presumptive diagnosis of past or current Legionnaires Disease.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 331706400001 / 99425-000025 / 885074698953 LIFEPAK 1000: The defibrillator is to be used in AED mode only on patients who are in cardiopulmonary arrest. The patient must be unresponsive, not breathing normally, and showing no signs of circulation. ECG monitoring is for use on conscious and unconscious patients of all ages for the purpose of ECG rhythm recognition and heart rate monitoring.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020 V15-2-001603 / 99577-001256 / 883873911631 LIFEPAK 15: The LP15 is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions. The LP15 is designed to be used during ground transportation except when specified otherwise. Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4,5F IV USA Model/Catalog Number: 5433742 Software Version: N/A Product Description: CELSITE BABYPORT SET PUR 4,5F IV USA Component: N/A
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
Plastic Trial Head Brown, 7 mm neck length. Item Number: 175-928/15.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
Prosthesis Head B, 28 mm, 7 mm neck length. Item Number: 198-828/04.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK, MODEL/ITEM NUMBER GRRB10E; 2) VAG HYST PACK, MODEL/ITEM NUMBER SPVH62P.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) A-C SUPPLEMENT PACK - 205946, Model/Item Number ANCV67X; 2) KIDNEY PERFUSION PACK - 208439, Model/Item Number ANKP15AD; 3) LAPCHOLAPPY PACK, Model/Item Number FYLA38G; 4) CYSTO PACK, Model/Item Number HSCY13M; 5) PICC DRESSING CHANGE KIT, Model/Item Number HSDR10K; 6) MIDLINE CHANGE KIT, Model/Item Number HSMD20H; 7) SHOULDER ARTHOSCOPY PACK, Model/Item Number PDSA12D; 8) PDA LF SJW, Model/Item Number SWPD12K; 9) AAA PACK - 206038, Model/Item Number UDAA63AH; 10) BASIC CAB PACK - 206043, Model/Item Number UDBC35AF; 11) BASIC HEART PACK - 206044, Model/Item Number UDBH37AX; 12) FREE FLAP DRAPE PACK (PS 907864), Model/Item Number UIFF72AD; 13) PROCUREMENT PACK, Model/Item Number UIPC89D; 14) THYROID PACK (PS 096552), Model/Item Number UITR45W; 15) TRAUMA PACK 175634, Model/Item Number UMTR17B; 16) TRAUMA PACK 175634, Model/Item Number UMTR17C.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) CYSTO, Model/Item Number ASCY24A; 2) CYSTO PACK, Model/Item Number BUCY78E; 3) CYSTO PACK, Model/Item Number LMCP22T; 4) TUR BASIN PACK, Model/Item Number LMTU31T; 5) CYSTO, Model/Item Number SACY80S; 6) UROLOGY PACK, Model/Item Number SPUR64F.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; All Software Versions.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) LAP CHOLE PACK, Model/Item Number CILC69L; 2) LAP CHOLE PACK, Model/Item Number HNLC80J; 3) LAP CHOLE PACK, Model/Item Number JKLC55H; 4) LAPAROSCOPY PACK, Model/Item Number LLLA21K; 5) GENERAL LAPAROSCOPY MPH, Model/Item Number MPGL15G;
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) HEART PACK - 205947, MODEL/ITEM NUMBER ANCV78BC; 2) VASCULAR PACK - 232024, MODEL/ITEM NUMBER ANVA82AB; 3) OFF PUMP CABG PACK - 170316, MODEL/ITEM NUMBER BHOP48O; 4) OFF PUMP CABG PACK - 170316, MODEL/ITEM NUMBER BHOP48P; 5) PEDIATRIC OPEN HEART PACK - 170212, MODEL/ITEM NUMBER BHPH18F; 6) PEDIATRIC OPEN HEART PACK - 170212, MODEL/ITEM NUMBER BHPH18G; 7) CABG ACCESSORY PACK, MODEL/ITEM NUMBER HGCB98F; 8) CV SET UP PACK, MODEL/ITEM NUMBER HGCV05K; 9) OPEN HEART PACK B - COMPONENTS, MODEL/ITEM NUMBER HGOH99H; 10) STRADLE TABLE PACK - 301659, MODEL/ITEM NUMBER MHCV10AM; 11) MINOR VASCULAR PACK, MODEL/ITEM NUMBER MTVS73D; 12) AV GRAFT RCH 0246952, MODEL/ITEM NUMBER RCAV40C; 13) OPEN HEART PART 1 RCH 0247159, MODEL/ITEM NUMBER RCOH61G; 14) CARDIO 612968, MODEL/ITEM NUMBER TNCA08T; 15) CV B PACK, MODEL/ITEM NUMBER TNCB10AM; 16) A-V FISTULA - 206042, MODEL/ITEM NUMBER UDAV16AD; 17) CAROTID PACK - 206045, MODEL/ITEM NUMBER UDCP24AF; 18) FEM POP PACK - 206052, MODEL/ITEM NUMBER UDFP36AH; 19) CARDIOVASCULAR SUPPLY (PS 907285), MODEL/ITEM NUMBER UICD62AN; 20) SFCH PEDS CARDIAC SUPPLY PACK (PS131653), MODEL/ITEM NUMBER UICS88S; 21) SFCH ECMO PACK (PS 107116), MODEL/ITEM NUMBER UIPD03Q; 22) THORACIC SETUP (PS 035700), MODEL/ITEM NUMBER UITC53AL; 23) VASCULAR PACK, MODEL/ITEM NUMBER UIVA75J; 24) CABG ACCESSORY PACK 175619, MODEL/ITEM NUMBER UMCA14E; 25) OPEN HEART ACCESS PACK 175628, MODEL/ITEM NUMBER UMOH42E; 26) OPEN HEART ACCESS PACK 175628, MODEL/ITEM NUMBER UMOH42F; 27) OPEN HEART ACCESS PACK 175628, MODEL/ITEM NUMBER UMOH42G.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) LAPAROSCOPY PACK, MODEL/ITEM NUMBER EVLP61I; 2) PELVISCOPY, MODEL/ITEM NUMBER EVPV29G.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) SFCH CRANI PACK (PS 132432), MODEL/ITEM NUMBER UICR10W; 2) SFCH SHUNT PACK (PS 139798), MODEL/ITEM NUMBER UISH55V.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ANTERIOR HIP PACK, MODEL/ITEM NUMBER AMAH40N; 2)TOTAL KNEE DAN MYER, MODEL/ITEM NUMBER CCKM67F; 3)HIP PROTHESIS PACK, MODEL/ITEM NUMBER HSTH03N; 4)DTC ANTERIOR HIP PACK (PS 209459), MODEL/ITEM NUMBER MIAH65B; 5)DR WHIDD0N TOTAL HIP CPP, MODEL/ITEM NUMBER MPWH01B; 6)KNEE ARTHROSCOPY, MODEL/ITEM NUMBER SPKA57T; 7)ANTERIOR HIP PACK, MODEL/ITEM NUMBER WVAH40H.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) BORN ON ARRIVAL KIT, Model/Item Number LLBN11C; 2) LABOR & DELIVERY PACK, Model/Item Number LLLD19I.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Device enforcement product
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
Review official root-cause evidence and provenance
? Unknown
An exact official-identifier join exists, but the joined records contain no supported root-cause wording. This is not an FDA finding of an unknown cause.
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
