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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

7,441 recalled products

2,526 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

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-S

Z-2071-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

Oxoid Agglutinating Sera, Salmonella 9-0 R30957301

Z-1923-2026 · initiated March 25, 2026

Unknown
Recalling firm
Remel Europe Ltd.
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98652
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

Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.

Z-1896-2026 · initiated March 25, 2026

Unknown
Recalling firm
Davol, Inc.
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98602
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

DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27

Z-2076-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25

Z-2078-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27

Z-2080-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-S

Z-2075-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

Heraeus, PALAMIX duo. Material Number: 66057897.

Z-1998-2026 · initiated March 25, 2026

Unknown
Classification
Class III
FDA status
Ongoing
Evidence destination
Event 98608
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

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S

Z-2079-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

Heraeus, PALAMIX uno. Material Number: 66057893.

Z-1997-2026 · initiated March 25, 2026

Unknown
Classification
Class III
FDA status
Ongoing
Evidence destination
Event 98608
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

DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23

Z-2069-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S

Z-2072-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25

Z-2074-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23

Z-2073-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25

Z-2070-2026 · initiated March 25, 2026

Unknown
Recalling firm
Katalyst Surgical, LLC
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98660
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

Yeastone Broth, 11ML, 10/BOX YY3462

Z-1806-2026 · initiated March 24, 2026

Unknown
Recalling firm
Remel, Inc
Classification
Class II
FDA status
Ongoing
Evidence destination
Event 98616
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

Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.

Z-2138-2026 · initiated March 24, 2026

Unknown
Recalling firm
Medline Industries, LP
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98735
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

Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. MTS,RT,HANDED/LFT,HRT,KIT, Medline Kit Number/SKU 60010508; 2. DBD-MTS,LEFT HEART,KIT, Medline Kit Number/SKU 60160075; 3. CARDIAC CATH PACK, Medline Kit Number/SKU DYNJ04636N; 4. CATH LAB TRAY, Medline Kit Number/SKU DYNJ24250G; 5. CATH LAB PACK-LF, Medline Kit Number/SKU DYNJ38333D; 6. CATH LAB PACK-LF, Medline Kit Number/SKU DYNJ38333F; 7. CATH LAB ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ50779G; 8. CATH LAB ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ50779I; 9. CLOT RETRIEVAL PACK, Medline Kit Number/SKU DYNJ56140C; 10. TAVR PACK NO SYR, Medline Kit Number/SKU DYNJ62310C; 11. TAVR PACK, Medline Kit Number/SKU DYNJ62310D; 12. TAVR PACK, Medline Kit Number/SKU DYNJ62310F; 13. DIAGNOSTIC 2 PACK, Medline Kit Number/SKU DYNJ81911; 14. DIAGNOSTIC 2 PACK, Medline Kit Number/SKU DYNJ81911A; 15. CATH PACK, Medline Kit Number/SKU DYNJT6544; 16. LHK, Medline Kit Number/SKU NAM0015; 17. SLU LHK, Medline Kit Number/SKU SAMPC0706.

Z-2147-2026 · initiated March 24, 2026

Unknown
Recalling firm
Medline Industries, LP
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98735
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

Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.

Z-2139-2026 · initiated March 24, 2026

Unknown
Recalling firm
Medline Industries, LP
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98735
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

Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer

Z-2142-2026 · initiated March 24, 2026

Unknown
Recalling firm
Medline Industries, LP
Classification
Class I
FDA status
Ongoing
Evidence destination
Event 98735
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