Recall events
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Event 71293
Event summary
Timeline bucket May 01, 2015
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Beaver-Visitec International Inc.
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
5 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 5
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic surgical kits
Z-1802-2015
Recall number Z-1802-2015
Initiated May 01, 2015
Classification Class II
Status Terminated
Quantity 621 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1802-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[55553]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Code information Lot Numbers: 3035614 3046205 3052693 3055885 3063181 3068806 3073917 3082315
Distribution pattern Nationwide Distribution including KY, GA, MI, and NJ.
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[12627]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 5
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584648 Ophthalmic surgical kits
Z-1803-2015
Recall number Z-1803-2015
Initiated May 01, 2015
Classification Class II
Status Terminated
Quantity 384 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1803-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[20413]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Code information Lot Numbers: 3038787 3046210 3061080 3078492 3093681 3095940 3108668
Distribution pattern Nationwide Distribution including KY, GA, MI, and NJ.
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[10047]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 5
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584649 Ophthalmic surgical kits
Z-1804-2015
Recall number Z-1804-2015
Initiated May 01, 2015
Classification Class II
Status Terminated
Quantity 585 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1804-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[24513]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Code information Lot Numbers: 3039720 3046211 3047770 3049473 3070763 3082330 3089827 3093682 3095941 3106407 3117874
Distribution pattern Nationwide Distribution including KY, GA, MI, and NJ.
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[13516]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 5
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584671 Ophthalmic surgical kits
Z-1805-2015
Recall number Z-1805-2015
Initiated May 01, 2015
Classification Class II
Status Terminated
Quantity 214 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1805-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[20411]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Code information Lot Numbers: 3045852 3053258 3063193 3068829
Distribution pattern Nationwide Distribution including KY, GA, MI, and NJ.
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[13790]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 5
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584676 Ophthalmic surgical kits
Z-1806-2015
Recall number Z-1806-2015
Initiated May 01, 2015
Classification Class II
Status Terminated
Quantity 268 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1806-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[24512]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Code information Lot Numbers: 3068113 3078510 3086351 3089841 3096796
Distribution pattern Nationwide Distribution including KY, GA, MI, and NJ.
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[10046]
FDA event record
· Exact recall-number query on openFDA
