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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93679

17 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 20, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
C.R. Bard 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

17 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 17

Bard Nasogastric Sump Tube with ENFit, 10Fr., 36in Long, REF EN0042100

Z-0790-2024
Recall number
Z-0790-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
3400 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113772, Lot/Serial Numbers: NGEQ3034, NGER3656, NGFX0154, NGGR1392, NGGT2088, NGHQ2161

Distribution pattern

US

device · product 2 of 17

Bard¿ Nasogastric Sump Tube with ENFit, 12Fr., 48in Long, REF EN0042120

Z-0791-2024
Recall number
Z-0791-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
6704 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113789, Lot/Serial Numbers: NGDU4227, NGDX0616, NGEQ3058, NGER3569, NGFN0711, NGFS4430, NGFT1895, NGFT5466, NGFU2448, NGFV1675, NGFW1843, NGFX0166, NGFY2526, NGGR2645, NGGT2116, NGHQ2394

Distribution pattern

US

device · product 3 of 17

Bard¿ Nasogastric Sump Tube with ENFit, 14Fr., 48in Long, REF EN0042140

Z-0792-2024
Recall number
Z-0792-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
17250 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113796, Lot/Serial Numbers: NGEP0376, NGEQ3035, NGES3428, NGES4109, NGEZ0663, NGFN4314, NGFQ4110, NGFR5254, NGFT0553, NGFT1825, NGFT5022, NGFU1876, NGFV1653, NGFV3456, NGFW1885, NGFX0155, NGFX2654, NGFX5523, NGGQ4983, NGGR2655, NGHR0048

Distribution pattern

US

device · product 4 of 17

Bard¿ Nasogastric Sump Tube with ENFit, 16Fr., 48in Long, REF EN0042160

Z-0793-2024
Recall number
Z-0793-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
16564 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113802, Lot/Serial Numbers: NGDU4226, NGEQ3059, NGER3655, NGEY1508, NGEY2686, NGEZ2776, NGFP0405, NGFS4370, NGFT5975, NGFU1797, NGFV1674, NGFV3527, NGFW1855, NGFX2682, NGFX5610, NGGV0790

Distribution pattern

US

device · product 5 of 17

Bard¿ Nasogastric Sump Tube with ENFit, 18Fr., 48in Long, REF EN0042180

Z-0794-2024
Recall number
Z-0794-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
37059 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113819, Lot/Serial Numbers: NGDT1997, NGES3427, NGES4095, NGFV0834, NGFV3461, NGFW1886, NGFX5524, NGFY2527, NGGT3565

Distribution pattern

US

device · product 6 of 17

Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000

Z-0795-2024
Recall number
Z-0795-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
39430 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113765, Lot/Serial Numbers: NGEV2409, NGEY1492, NGEY2717, NGEZ0908, NGEZ1657, NGEZ2692, NGFQ4105, NGFR1077, NGFR2312, NGFR3259, NGFS1627, NGFS4431, NGFT5468, NGFU1877, NGFU3837, NGFV1652, NGFV3513, NGFW1856, NGFX0167, NGFX2672, NGFX5611, NGGP3169, NGGT3611

Distribution pattern

US

device · product 7 of 17

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 10Fr., 36in Long, REF EN0046100

Z-0796-2024
Recall number
Z-0796-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
6600 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113222, Lot/Serial Numbers: NGDX0768, NGDZ3314, NGER3568, NGFT5023, NGFV3443, NGFW1904, NGFX0156, NGFX5525, NGGQ8459, NGGW4504

Distribution pattern

US

device · product 8 of 17

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit", 12Fr., 48in Long, REF EN0046120

Z-0797-2024
Recall number
Z-0797-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
26100 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113239, Lot/Serial Numbers: NGDT1998, NGDZ3287, NGEU0889, NGEU2134, NGEV2411, NGEW2655, NGEY1506, NGEZ0664, NGFN4265, NGFU4024, NGFV3514, NGFW1857, NGFX0168, NGFX2645, NGGQ8458, NGGR2705, NGGX4777

Distribution pattern

US

device · product 9 of 17

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 14Fr., 48in Long, REF EN0046140

Z-0798-2024
Recall number
Z-0798-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
36440 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113246, Lot/Serial Numbers: NGDT1999, NGDU4285, NGDX0617, NGES3429, NGET1383, NGEU2115, NGEV4551, NGEX1978, NGEY0623, NGEY2687, NGFN0745, NGFN4316, NGFQ4111, NGFV3444, NGFW1905, NGFX2673, NGFX5526, NGGT4255, NGGU4246, NGGX5757

Distribution pattern

US

device · product 10 of 17

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 16Fr., 48in Long, REF EN0046160

Z-0799-2024
Recall number
Z-0799-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
51750 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113253, Lot/Serial Numbers: NGDX0520, NGES3426, NGET0807, NGET1424, NGEX0089, NGEX1018, NGEY0581, NGEZ0909, NGEZ2672, NGFN1384, NGFN2360, NGFP3401, NGFS4432, NGFT1896, NGFT3418, NGFT5962, NGFV3515, NGFW1858, NGFX0157, NGFX5613, NGGP3235, NGGR2656, NGGX5810, NGHP2260

Distribution pattern

US

device · product 11 of 17

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 18Fr., 48in Long, REF EN0046180

Z-0800-2024
Recall number
Z-0800-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
57159 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113260, Lot/Serial Numbers: NGDT2000, NGDX0518, NGEW1822, NGEW3855, NGEX0043, NGEX1998, NGEZ2693, NGFP0406, NGFP3519, NGFR0244, NGFT0418, NGFT3481, NGFU3821, NGFV0785, NGFV1654, NGFV3445, NGFW1906, NGFX0169, NGFX2674, NGFX5527, NGGP3171

Distribution pattern

US

device · product 12 of 17

Bard¿ Lopez Valve¿ with ENFit, REF EN0056000

Z-0801-2024
Recall number
Z-0801-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
187550 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113901, Lot/Serial Numbers: NGFU2486, NGFU3807, NGFW1859, NGFX0062, NGFX5625, NGFY0610, NGFZ1664, NGGR0346, NGGR2172, NGGS0703, NGGS2557, NGGS3418, NGGYY001, NGHN0893, NGHQ3357, NGHQ3358, NGHQ3359, NGHQ3383, NGHQ3384, NGHR0028, NGHR0029, NGHR0030, NGHR0031, NGHR0032, NGHR0072, NGHR0073, NGHR0074, NGHR0075, NGHR0159, NGHV0889, NGHV2621, NGHV2722, NGHV3877, NGHW0569, NGHW1488, NGHW3036, NGHW4578, NGHX0643, NGHX0869

Distribution pattern

US

device · product 13 of 17

Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 12Fr., 48in Long, REF EN0056120

Z-0802-2024
Recall number
Z-0802-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
3360 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113840, Lot/Serial Numbers: NGDU4228, NGGR2707

Distribution pattern

US

device · product 14 of 17

Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 14Fr., 48in Long, REF EN0056140

Z-0803-2024
Recall number
Z-0803-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
3650 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113857, Lot/Serial Numbers: NGEX0090, NGEX1982, NGEZ2116, NGGP3242, NGHQ1395, NGHQ1411

Distribution pattern

US

device · product 15 of 17

Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 16Fr., 48in Long , REF EN0056160

Z-0804-2024
Recall number
Z-0804-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
8010 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113864, Lot/Serial Numbers: NGDU4284, NGEP0365, NGER3654, NGGR2706, NGGT2087, NGHW4543

Distribution pattern

US

device · product 16 of 17

Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 18Fr., 48in Long, REF EN0056180

Z-0805-2024
Recall number
Z-0805-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
9860 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741113871, Lot/Serial Numbers: NGDU4286, NGDX0519, NGES3430, NGET0635, NGEY1509, NGFN0746, NGFQ4112, NGFR2309, NGFT3419, NGFX5614, NGGP3176, NGHS0685, NGHS2419, NGHT2751

Distribution pattern

US

device · product 17 of 17

Bard¿ Suction Connector with ENFit, REF EN0066000

Z-0806-2024
Recall number
Z-0806-2024
Initiated
December 20, 2023
Classification
Class II
Status
Ongoing
Recalling firm
C.R. Bard Inc
Quantity
133610 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Code information

UDI/DI 00801741128707, Lot/Serial Numbers: NGFS2792, NGFS4371, NGFV1647, NGFV1669, NGGN1988, NGGN2930, NGGN3517, NGGP0451, NGGP1098, NGGV0739, NGGV2722, NGGV5069, NGGW4456, NGGX3169, NGGZ0564, NGGZ1915, NGHP2225, NGHQ2201, NGHR0090, NGHS1005, NGHS1006, NGHS2421, NGHS3331, NGHU0845, NGHU1555, NGHV0467, NGHV2758, NGHW3025, NGHX1021, NGHX3269

Distribution pattern

US

Field note

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