Recall events
/
Event 95909
Event summary
Timeline bucket October 22, 2024
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Carwild Corporation
Dossier provenance
Source snapshots represented here
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.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
3 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 3
Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site. Model Number: Q604206
Z-0798-2025
Recall number Z-0798-2025
Initiated October 22, 2024
Classification Class II
Status Ongoing
Quantity 120 units
App-derived interpretation
Potency or specification failure
reason.potency_specification_failure · v1.0.0
out of specification
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Equipment maintenance
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0798-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29403]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Code information LOT NUMBER: 24G1880
Distribution pattern IL, FL, SC. PA, AL Foreign: Netherlands
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[3908]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 3
Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During Ophthalmic Surgical Procedures For Fluid Management Model Number: Q604237
Z-0799-2025
Recall number Z-0799-2025
Initiated October 22, 2024
Classification Class II
Status Ongoing
Quantity 300 units
App-derived interpretation
Potency or specification failure
reason.potency_specification_failure · v1.0.0
out of specification
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Equipment maintenance
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0799-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17379]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Code information LOT NUMBER: 24G1739
Distribution pattern IL, FL, SC. PA, AL Foreign: Netherlands
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[3732]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 3
Ivalon Anatomical Nasal Packing with Airway Tube and String, 8.0 cm x 1.5cmx 3.0 cm- Intended To Be Used During Ophthalmic Surgical Procedures For Fluid Management Model Number: Q770410
Z-0800-2025
Recall number Z-0800-2025
Initiated October 22, 2024
Classification Class II
Status Ongoing
Quantity 140 units
App-derived interpretation
Potency or specification failure
reason.potency_specification_failure · v1.0.0
out of specification
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Equipment maintenance
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0800-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40787]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Code information LOT NUMBER: 24F1638
Distribution pattern IL, FL, SC. PA, AL Foreign: Netherlands
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[3656]
FDA event record
· Exact recall-number query on openFDA
